| Diseases |
Alias |
|
| Squamous Cell Carcinoma, Head And Neck |
|
Squamous Cell Carcinoma Of The Head And Neck
|
HNSCC
|
|
Head And Neck Squamous Cell Carcinoma
|
Head And Neck Cancer
|
|
Squamous Cell Carcinoma Of Lip
|
Squamous Cell Carcinoma, Head And Neck, Somatic
|
|
Carcinoma Of The Head And Neck
|
Squamous Cell Carcinomas Of Head And Neck
|
|
Scchn
|
Squamous Cell Carcinoma Of The Hypopharynx
|
|
Squamous Cell Carcinoma Of The Oropharynx
|
Squamous Cell Carcinoma Of Salivary Glands
|
|
Squamous Cell Carcinoma Of The Nasal Cavity And Paranasal Sinuses
|
Squamous Cell Carcinoma Of The Nasal Cavity And Sinuses
|
|
Squamous Cell Carcinoma Of The Oral Cavity
|
Squamous Cell Carcinoma Of The Lip
|
|
Carcinoma, Squamous Cell Of Head And Neck
|
Lip Squamous Cell Carcinoma
|
|
Cancer, Head/Neck
|
Carcinoma, Squamous Cell, Head And Neck
|
|
Salivary Gland Squamous Cell Carcinoma
|
Cancer Of Head And Neck
|
|
Squamous Cell Carcinoma Of Oropharynx Nos
|
|
|
| Urinary Tract Papillary Transitional Cell Benign Neoplasm |
|
Inverted Papilloma Of Urinary Tract
|
Papillary Transitional Cell Neoplasm Of The Urinary Tract
|
|
Urinary Tract Inverted Papilloma
|
Inverted Urothelial Papilloma
|
|
|
| Kallmann Syndrome |
|
Hypogonadism With Anosmia
|
Kallman'S Syndrome
|
|
Anosmic Hypogonadism
|
Anosmic Idiopathic Hypogonadotropic Hypogonadism
|
|
Hypogonadotropic Hypogonadism And Anosmia
|
Hypogonadotropic Hypogonadism-Anosmia Syndrome
|
|
Olfacto-Genital Pathological Sequence
|
Familial Hypogonadism With Anosmia
|
|
Kallman Syndrome
|
Dysplasia Olfactogenitalis Of De Morsier
|
|
Kallmann'S Syndrome
|
Congenital Hypogonadotropic Hypogonadism With Anosmia
|
|
|
| Renal Hypodysplasia/Aplasia 3 |
|
RHDA3
|
Renal Agenesis, Unilateral
|
|
Unilateral Renal Agenesis
|
|
|
| Schimmelpenning-Feuerstein-Mims Syndrome |
|
Nevus Sebaceus Of Jadassohn
|
Organoid Nevus Phakomatosis
|
|
Linear Nevus Sebaceous Syndrome
|
Sfm Syndrome
|
|
Jadassohn Nevus Phakomatosis
|
Jnp
|
|
Schimmelpenning Syndrome
|
Solomon Syndrome
|
|
SFM
|
Linear Sebaceous Nevus Syndrome
|
|
Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic
|
Nevus Sebaceus Syndrome
|
|
Organoid Nevus Syndrome
|
Schimmelpenning Feuerstein Mims Syndrome
|
|
Sebaceous Nevus Syndrome, Linear
|
Epidermal Nevus Syndrome, Formerly
|
|
Sebaceous Nevus Syndrome Linear
|
Linear Nevus Sebaceus Syndrome
|
|
Epidermal Nevus Syndrome
|
Ss
|
|
Nevus Sebaceous
|
|
|
| Keratosis, Seborrheic |
|
Seborrheic Keratosis
|
Keratosis, Seborrheic, Somatic
|
|
Basal Cell Papilloma
|
Keratosis Seborrheica
|
|
KERSEB
|
|
|
| Dacryocystocele |
|
|
| Achondroplasia |
|
Achondroplastic Dwarfism
|
ACH
|
|
Osteosclerosis Congenita
|
Achondroplastic Physique
|
|
Chondrodystrophia
|
Dwarf, Achondroplastic
|
|
Achondroplastic Short Stature
|
Congenital Osteosclerosis
|
|
|
| Scoliosis |
|
|
| Porokeratosis |
|
Disseminated Superficial Actinic Porokeratosis
|
Dsap
|
|
Porokeratosis Of Mibelli
|
Porokeratosis, Disseminated Superficial Actinic
|
|
Porokeratosis, Disseminated Superficial Actinic, 1
|
|
|
| Dermatosis Papulosa Nigra |
|
|
| Squamous Cell Carcinoma |
|
Epidermoid Carcinoma
|
Squamous Cell Cancer
|
|
Carcinoma, Squamous Cell
|
Malignant Squamous Cell Tumor
|
|
Squamous Carcinoma
|
Squamous Cell Epithelioma
|
|
Squamous Cell Skin Cancer
|
Carcinoma Squamous Cell
|
|
Neoplasms, Squamous Cell
|
Squamous Cell Carcinoma - Category
|
|
Malignant Squamous Cell Neoplasm
|
Squamous Cell Carcinoma Of Skin
|
|
|
| Plasma Cell Leukemia |
|
Plasma Cell Leukaemia
|
Leukemia, Plasma Cell
|
|
Plasmacytic Leukaemia
|
Plasmacytic Leukemia
|
|
Pcl
|
Plasma Cell Leukaemia, Nos
|
|
Leukemic Plasma Cell
|
Plasma Cell Leukaemia Without Mention Of Remission
|
|
|
| Craniosynostosis |
|
Premature Closure Of Cranial Sutures
|
Craniostenosis
|
|
Craniosynostosis Syndrome
|
Cso
|
|
Craniosynostoses
|
Congenital Ossification Of Cranial Sutures
|
|
Congenital Ossification Of Sutures Of Skull
|
Craniostosis
|
|
Imperfect Fusion Of Skull
|
Congenital Imperfect Closure Skull
|
|
Imperfect Closure Skull
|
Premature Closure Cranium Sutures
|
|
Deficiency Of Craniofacial Axis
|
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Lung Cancer Susceptibility 3 |
|
Lung Adenocarcinoma
|
Adenocarcinoma Of Lung
|
|
LNCR3
|
Adenocarcinoma Of Lung, Susceptibility To
|
|
Bronchogenic Lung Adenocarcinoma
|
Nonsmall Cell Adenocarcinoma
|
|
Adenocarcinoma Lung
|
Lung Adenocarcinomas
|
|
Non-Small Cell Adenocarcinoma
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans |
|
SADDAN
|
Saddan Dysplasia
|
|
Severe Achondroplasia-Developmental Delay-Acanthosis Nigricans Syndrome
|
Severe Achondroplasia With Developmental Delay And Acanthosis Nigricans
|
|
Ssb Syndrome
|
Skeleton Skin Brain Syndrome
|
|
Skeleton-Skin-Brain Syndrome
|
Achondroplasia
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Bladder Transitional Cell Papilloma |
|
Bladder Papilloma
|
Transitional Cell Papilloma Of Bladder
|
|
Urinary Bladder Urothelial Papilloma
|
Urothelial Papilloma
|
|
Bladder Urothelial Papilloma
|
|
|
| Chondrosarcoma |
|
Cartilaginous Cancer
|
Chondrosarcoma Of Bone
|
|
Primary Chondrosarcoma Of The Bone
|
CHDSA
|
|
|
| Primary Bone Dysplasia |
|
Primary Osteodysplasia
|
Primary Skeletal Dysplasia
|
|
|
| Sarcomatoid Transitional Cell Carcinoma |
|
Transitional Cell Carcinoma, Sarcomatoid
|
Transitional Spindle Cell Carcinoma
|
|
Transitional Cell Carcinoma, Spindle Cell
|
|
|
| Osteochondroma |
|
|
| Achondrogenesis |
|
|
| Spermatocytoma |
|
|
| Transitional Cell Carcinoma |
|
Transitional Cell Neoplasm
|
Carcinoma, Transitional Cell
|
|
Transitional Carcinoma
|
Transitional Cell Tumor
|
|
Urothelial Cell Carcinoma
|
Carcinoma Transitional Cell
|
|
Transitional Cell Carcinoma Of Bladder
|
|
|
| Osteoglophonic Dysplasia |
|
Osteoglophonic Dwarfism
|
OGD
|
|
Fairbank-Keats Syndrome
|
Osteoglosphonic Dysplasia
|
|
Dysplasia, Osteoglophonic
|
|
|
| Hepatoblastoma |
|
|
| Ureter, Cancer Of |
|
Ureter Carcinoma
|
Ureter Cancer
|
|
Ureteral Neoplasms
|
Malignant Neoplasm Of Ureter
|
|
Malignant Tumour Of Ureter
|
Malignant Ureteral Tumor
|
|
Ureteral Carcinoma
|
Ureteral Neoplasm
|
|
|
| Skin Benign Neoplasm |
|
Neoplasm Of Skin By Site
|
Tumor Of The Skin
|
|
Skin Tumor
|
Benign Neoplasm Of Skin
|
|
Skin Neoplasms
|
|
|
| Muenke Syndrome |
|
Muenke Nonsyndromic Coronal Craniosynostosis
|
Fgfr3-Related Craniosynostosis
|
|
Fgfr3-Associated Coronal Synostosis
|
Coronal Craniosynostosis
|
|
MNKES
|
Syndrome Of Coronal Craniosynostosis
|
|
MNKS
|
Fgfr3-Related Isolated Coronal Synostosis
|
|
Muenke Non-Syndromic Coronal Craniosynostosis
|
|
|
| Acromesomelic Dysplasia 1 |
|
Acromesomelic Dysplasia, Maroteaux Type
|
Amdm
|
|
Acromesomelic Dysplasia 1, Maroteaux Type
|
AMD1
|
|
St. Helena Dysplasia
|
Acromesomelic Dysplasia Maroteaux Type
|
|
Acromesomelic Dwarfism Maroteux Type
|
Dysplasia, Acromesomelic, Type 1, Maroteaux
|
|
Acromesomelic Dysplasia Hunter-Thompson Type
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Protection Against
|
Lung Cancer, Susceptibility To
|
|
Adenocarcinoma Of Lung, Somatic
|
Nonsmall Cell Lung Cancer
|
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Endometrial Cancer |
|
Endometrial Carcinoma
|
Endometrial Neoplasm
|
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
|
ENDMC
|
Carcinoma Endometrioid
|
|
Endometrial Cancers
|
Cancer, Endometrial
|
|
Uterine Corpus Cancer
|
|
|
| Sensorineural Hearing Loss |
|
Sensory Hearing Loss
|
Sensorineural Hearing Loss Disorder
|
|
Hearing Loss, Sensorineural
|
Central Hearing Loss
|
|
High Frequency Deafness
|
High Frequency Hearing Loss
|
|
High-Frequency Hearing Loss
|
Perceptive Deafness
|
|
Perceptive Hearing Loss
|
Perceptive Hearing Loss Or Deafness
|
|
Sensorineural Deafness
|
Hearing Loss Sensorineural
|
|
Deafness Sensorineural
|
Hearing Loss High-Frequency
|
|
Hearing Loss, Central
|
Hearing Loss, High-Frequency
|
|
|
| Strabismus |
|
Strabismus, Susceptibility To
|
Strabismus, Susceptibility To, 1
|
|
Strabismus 1
|
|
|
| Cherubism |
|
CRBM
|
Familial Benign Giant-Cell Tumor Of The Jaw
|
|
Familial Fibrous Dysplasia Of Jaw
|
Familial Multilocular Cystic Disease Of The Jaws
|
|
|
| Renal Cell Carcinoma, Papillary, 1 |
|
Papillary Renal Cell Carcinoma
|
Hereditary Papillary Renal Cell Carcinoma
|
|
Papillary Renal Cell Carcinoma, Sporadic
|
Papillary Renal Cell Adenocarcinoma
|
|
RCCP
|
RCCP1
|
|
Renal Cell Carcinoma, Papillary
|
Renal Cell Carcinoma, Papillary, 1, Familial And Somatic
|
|
Chromophil Carcinoma Of Kidney
|
Papillary Kidney Carcinoma
|
|
Sporadic Papillary Renal Cell Carcinoma
|
Chromophil Renal Cell Carcinoma
|
|
Papillary Renal Carcinoma, Malignant -
|
Papillary Renal Cell Carcinoma, Bilateral -
|
|
Papillary Renal Cell Carcinoma, Familial -
|
Papillary Renal Cell Carcinoma, Multiple -
|
|
Papillary Renal Cell Carcinoma, Sporadic -
|
Renal Adenocarcinoma
|
|
Chromophil Rcc
|
Hprcc
|
|
Renal Cell Carcinoma Papillary
|
Chromophilic Renal Cell Carcinoma
|
|
Prcc
|
Carcinoma, Renal Cell, Papillary, Type 1
|
|
Type 1 Papillary Renal Cell Carcinoma
|
Renal Cell Carcinoma
|
|
Hereditary Papillary Renal Carcinoma
|
|
|
| Bone Development Disease |
|
|
| Down Syndrome |
|
Trisomy 21
|
Complete Trisomy 21 Syndrome
|
|
Down'S Syndrome
|
Trisomy 21 Syndrome
|
|
Down'S Syndrome - Trisomy 21
|
Downs Syndrome
|
|
G Trisomy
|
47,Xx,+21
|
|
47,Xy,+21
|
Trisomy G
|
|
Down Syndrome, Susceptibility To
|
Chromosome 21 Trisomy
|
|
Trisomy 21 Nos
|
Abnormal Autosomes 21
|
|
|
| Gastrointestinal Stromal Tumor |
|
GIST
|
Gastrointestinal Stromal Tumors
|
|
Gastrointestinal Stromal Sarcoma
|
Gastrointestinal Stromal Tumor, Familial
|
|
Gant
|
Gastrointestinal Stromal Tumour
|
|
Stromal Tumor Of Gastrointestinal Tract
|
Stromal Tumour Of Gastrointestinal Tract
|
|
Gastrointestinal Stromal Neoplasm
|
Paraganglioma And Gastric Stromal Sarcoma
|
|
Plexosarcoma
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Testicular Germ Cell Tumor |
|
Male Germ Cell Tumor
|
Testicular Teratoma
|
|
TGCT
|
Mgct
|
|
Male Germ Cell Tumor, Somatic
|
Spermatocytic Seminoma, Somatic
|
|
Embryonal Cell Carcinoma
|
Seminoma
|
|
Spermatocytic Seminoma
|
Germ Cell Tumors, Somatic
|
|
Testicular Tumor, Somatic
|
Non-Seminomatous Germ Cell Tumor Of Testis
|
|
Non-Dysgerminomatous Germ Cell Tumor Of Testis
|
Testicular Non Seminomatous Germ Cell Tumor
|
|
Testicular Non-Dysgerminomatous Germ Cell Tumor
|
Teratoma Of The Testis
|
|
Endodermal Sinus Tumor
|
Nonseminomatous Germ Cell Tumors
|
|
Teratoma Testicular
|
Germ Cell Tumor, Somatic
|
|
Embryonal Carcinoma Cell
|
Yolk Sac Tumor
|
|
Malignant Testicular Non-Seminomatous Germ Cell Tumor
|
Testicular Non-Seminomatous Germ Cell Tumor
|
|
Teratoma Of Testis
|
Nonseminomatous Germ Cell Tumor
|
|
|
| Thanatophoric Dysplasia, Type Ii |
|
TD2
|
Thanatophoric Dysplasia With Kleeblattschaedel
|
|
Cloverleaf Skull With Thanatophoric Dwarfism
|
Thanatophoric Dysplasia With Straight Femurs And Cloverleaf Skull
|
|
Thanatophoric Dysplasia Type 2
|
Cloverleaf Skull-Micromelic Bone Dysplasia Syndrome
|
|
Thanatophoric Dwarfism Type 2
|
Thanatophoric Dwarfism-Cloverleaf Skull Syndrome
|
|
Thanatophoric Dysplasia Type Ii
|
Thanatophoric Dysplasia, Type 2
|
|
Thanatophoric Dwarfism - Cloverleaf Skull
|
Thanatophoric Dysplasia 2
|
|
|
| Bladder Urothelial Carcinoma |
|
Bladder Transitional Cell Carcinoma
|
Transitional Cell Carcinoma Of Bladder
|
|
Transitional Cell Carcinoma Of The Bladder
|
Urinary Bladder Urothelial Carcinoma
|
|
Urothelial Bladder Carcinoma
|
Carcinoma Transitional Cell Bladder
|
|
Tcc - [Transitional Cell Carcinoma] Of Bladder
|
|
|
| Pfeiffer Syndrome |
|
Infectious Mononucleosis
|
Acs5
|
|
Craniofacial-Skeletal-Dermatologic Dysplasia
|
Acs V
|
|
Noack Syndrome
|
Gammaherpesviral Mononucleosis
|
|
Acrocephalosyndactyly Type 5
|
Pfeiffer Syndrome Type 3
|
|
Acrocephalosyndactyly, Type V
|
Glandular Fever
|
|
Pfeiffer Type Acrocephalosyndactyly
|
Pfeiffer Syndrome Type 2
|
|
Acrocephalosyndactylia Type V
|
Filatov'S Disease
|
|
Monocytic Angina
|
Mononucleosis
|
|
Pfeiffer'S Disease
|
Acsv
|
|
Acrocephalosyndactyly, Type 5
|
Craniofacial-Skeletal-Dermatologic Syndrome
|
|
Pfeiffer Syndrome Type 1
|
Classic Pfeiffer Syndrome
|
|
PS
|
Pfeiffer Syndrome Variant
|
|
Dysplasia, Craniofacial-Skeletal-Dermatologic
|
Pfeiffer
|
|
Kissing Disease
|
Infectious Adenitis
|
|
Pfeiffer Disease
|
|
|
| Skin Disease |
|
Skin Diseases
|
Abnormality Of The Skin
|
|
Skin Diseases, Genetic
|
Genodermatosis
|
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
| Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations |
|
Spondyloepiphyseal Dysplasia
|
Chst3-Related Skeletal Dysplasia
|
|
Humerospinal Dysostosis
|
Spondyloepiphyseal Dysplasia, Omani Type
|
|
Chondrodysplasia With Multiple Dislocations
|
SEDCJD
|
|
Hsd
|
Cdmd
|
|
Kozlowski Celermajer Tink Syndrome
|
Chondrodysplasia With Congenital Joint Dislocations, Chst3 Type
|
|
Larsen Syndrome, Recessive Type
|
Humero-Spinal Dysostosis With Congenital Heart Disease
|
|
Omani Type
|
Sed
|
|
Chst3 Deficiency
|
Chst3-Related Dysplasia
|
|
Recessive Larsen Syndrome
|
Autosomal Recessive Larsen Syndrome
|
|
Humero-Spinal Dysostosis
|
Sed With Luxations, Chst3 Type
|
|
Sed, Omani Type
|
Sdcd, Chst3 Type
|
|
Spondyloepiphyseal Dysplasia With Congenital Joint Dyslocations, Chst3 Type
|
Sed Omani Type
|
|
Spondyloepiphyseal Dysplasia Omani Type
|
Larsen Syndrome, Autosomal Recessive
|
|
Mucopolysaccharidosis Iv
|
Spondyloepiphyseal Dysplasia, Congenita
|
|
|
| Familiar Ovarian Carcinoma |
|
|
| Testicular Spermatocytic Seminoma |
|
|
| Wolf-Hirschhorn Syndrome |
|
Pitt-Rogers-Danks Syndrome
|
WHS
|
|
Chromosome 4p16.3 Deletion Syndrome
|
Wittwer Syndrome
|
|
4p- Syndrome
|
Pitt Syndrome
|
|
4p Deletion Syndrome
|
Distal Deletion 4p
|
|
Distal Monosomy 4p
|
Telomeric Deletion 4p
|
|
Prds
|
4p Syndrome
|
|
Chromosome 4p Syndrome
|
Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation
|
|
Wolf Syndrome
|
Chromosome 4p Deletion Syndrome
|
|
Chromosome 4p Monosomy
|
Del Syndrome
|
|
Monosomy 4p
|
Partial Monosomy 4p
|
|
Chromosome 4 Short Arm Deletion
|
|
|
| Hemifacial Hyperplasia |
|
Facial Asymmetry
|
Hemifacial Hypertrophy
|
|
Facial Hemihypertrophy
|
Asymmetric Face
|
|
|
| Chronic Inflammation Of Lacrimal Passage |
|
|
| Chiari Malformation |
|
|
| Epidermolytic Nevus |
|
Epidermolytic Epidermal Nevus
|
Epidermal Nevus With Epidermolytic Hyperkeratosis
|
|
Epidermolytic Verrucous Epidermal Nevus
|
|
|
| Exophthalmos |
|
|
| Isolated Growth Hormone Deficiency, Type Ia |
|
Ighd Ia
|
Isolated Growth Hormone Deficiency Type Ia
|
|
Primordial Dwarfism
|
Sexual Ateleiotic Dwarfism
|
|
Pituitary Dwarfism I
|
IGHD1A
|
|
Illig-Type Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated, Type Ia
|
|
Congenital Ighd Type Ia
|
Congenital Isolated Gh Deficiency Type Ia
|
|
Congenital Isolated Growth Hormone Deficiency Type Ia
|
Pituitary Dwarfism 1
|
|
Growth Hormone Deficiency, Isolated, Autosomal Recessive
|
Autosomal Recessive Isolated Growth Hormone Deficiency
|
|
Isolated Growth Hormone Deficiency Type 1a
|
Congenital Ighd
|
|
Congenital Isolated Gh Deficiency
|
Congenital Isolated Growth Hormone Deficiency
|
|
Growth Hormone Deficiency, Isolated Autosomal Recessive
|
Illig Type Growth Hormone Deficiency
|
|
Non-Acquired Isolated Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated, 1a
|
|
Growth Hormone Deficiency Isolated Autosomal Recessive
|
Dwarfism, Primordial
|
|
Dwarfism
|
|
|
| Adenocarcinoma |
|
Adenocarcinomas
|
Adenoacanthoma Of Unspecified Site
|
|
Adenocarcinoid Of Unspecified Site
|
Adenocarcinoid Tumour Of Unspecified Site
|
|
Adenocarcinoma And Carcinoid Combined Of Unspecified Site
|
Adenocarcinoma Nos
|
|
|
| Pectus Excavatum |
|
Funnel Chest
|
Congenital Pectus Excavatum
|
|
|
| Nevus, Epidermal |
|
Epidermal Nevus
|
Woolly Hair Nevus
|
|
Epidermal Naevus
|
Epidermal Nevus Syndrome
|
|
Nevus, Keratinocytic, Nonepidermolytic
|
Epidermal Nevus, Somatic
|
|
Nevus, Epidermal, Somatic
|
Nevus Sebaceous Or Woolly Hair Nevus, Somatic
|
|
Nonepidermolytic Keratinocytic Nevus
|
Epidermal Hamartoma Syndrome
|
|
Wooly Hair Nevus
|
Keratinocytic Non-Epidermolytic Nevus
|
|
KNEN
|
Pigmented Moles
|
|
Organoid Nevus Phakomatosis
|
Nevus Sebaceous
|
|
Melanocytic Nevus
|
Melanocytic Nevus Of Skin
|
|
|
| Thanatophoric Dysplasia, Type I |
|
Thanatophoric Dysplasia
|
Thanatophoric Dwarfism
|
|
Thanatophoric Dysplasia Type 1
|
TD1
|
|
Td
|
Thanatophoric Short Stature
|
|
Thanatophoric Dwarfism Type 1
|
Thanatophoric Dysplasia Type I
|
|
Platyspondylic Lethal Skeletal Dysplasia, San Diego Type
|
Lethal Short-Limbed Platyspondylic Dwarfism, San Diego Type
|
|
Skeletal Dysplasia, San Diego Type
|
Plsd San Diego Type
|
|
Thanatophoric Dwarfism 1
|
Dwarfism Thanatophoric
|
|
Dwarf, Thanatophoric
|
Thanatophoric Dysplasia 1
|
|
Lethal Short-Limbed Platyspondylic Dwarfism San Diego Type
|
Platyspondylic Lethal Skeletal Dysplasia San Diego Type
|
|
Thanatophoric Dwarf
|
Thanatophoric Dwarfism Or Short Stature
|
|
Thanatophoric Dwarfism Syndrome
|
Td - [Thanatophoric Dwarfism]
|
|
|
| Germ Cell Tumor |
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Acanthoma |
|
|
| Monoclonal Gammopathy Of Uncertain Significance |
|
Monoclonal Gammopathy Of Undetermined Significance
|
Mgus
|
|
Mgus - [Monoclonal Gammopathy Of Undetermined Significance]
|
Monoclonal Gammopathy Nos
|
|
Iga Gammopathy
|
Monoclonal Gammoglobulinopathy
|
|
|
| Squamous Blepharitis |
|
|
| Pigmentation Disease |
|
Pigmentation Disorders
|
Skin Pigmentation Disorder
|
|
|
| Hypophosphatemic Rickets, X-Linked Dominant |
|
Xlh
|
Vitamin D-Resistant Rickets, X-Linked
|
|
X-Linked Hypophosphatemia
|
XLHR
|
|
Hyp
|
Hypophosphatemic Vitamin D-Resistant Rickets
|
|
Hpdr
|
X-Linked Hypophosphatemic Rickets
|
|
X-Linked Dominant Hypophosphatemic Rickets
|
Familial Hypophosphatemic Rickets
|
|
Hypophosphatemia, X-Linked
|
Hypophosphatemia, Vitamin D-Resistant Rickets
|
|
Hypophosphatemic Rickets X-Linked Dominant
|
X-Linked Vitamin D-Resistant Rickets
|
|
Hypophophatemia, X-Linked
|
Hypophophatemic Vitamin D-Resistant Rickets
|
|
Hypophosphatemia X-Linked
|
Vitamin D-Resistant Rickets X-Linked
|
|
Vitamin D-Resistant Rickets
|
Rickets, X-Linked Hypophosphatemic
|
|
|
| Bladder Papillary Transitional Cell Neoplasm |
|
Urinary Bladder Papillary Urothelial Neoplasm
|
Bladder Papillary Urothelial Neoplasm
|
|
|
| Pseudohypoparathyroidism |
|
Familial Pseudohypoparathyroidism
|
Parathyroid Hormone Resistant Hypoparathyroidism
|
|
Php - [Pseudohypoparathyroidism]
|
Constitutional Chronic Hypocalcaemia
|
|
|
| Acanthosis Nigricans |
|
|
| Papilloma |
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Syndactyly, Type I
|
|
Sd1
|
Zygodactyly
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Non-Syndromic Syndactyly
|
|
Symphalangism
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| Larsen Syndrome |
|
LRS
|
Larsen Syndrome, Dominant Type
|
|
Dominant Larsen Syndrome
|
Autosomal Dominant Larsen Syndrome
|
|
Larsens Syndrome
|
|
|
| Cervical Cancer |
|
Cervical Cancer, Somatic
|
Neoplasm Of Uterine Cervix
|
|
Cervix Cancer
|
Uterine Cervical Neoplasm
|
|
Cervical Neoplasm
|
Cervix Uteri Cancer
|
|
Tumor Of The Cervix Uteri
|
CERCA
|
|
Uterine Cervical Cancer
|
Neoplasms Cervical
|
|
Uterine Cervical Neoplasms
|
Cervical Cancers
|
|
Cancer, Cervical, Somatic
|
Malignant Tumor Of Cervix
|
|
Cervix Carcinoma
|
|
|
| Plagiocephaly |
|
Asymmetric Head
|
Lateral Curvatures Of Skull Unequal
|
|
Unicoronal Synostosis
|
|
|
| Cheilitis |
|
|
| Non-Invasive Bladder Papillary Urothelial Neoplasm |
|
Bladder Papillary Neoplasm Of Low Malignant Potential
|
Bladder Punlmp
|
|
Papillary Urothelial Neoplasm Of Low Malignant Potential
|
Papillary Transitional Cell Neoplasm Of Low Malignant Potential
|
|
|
| Giant Cell Glioblastoma |
|
|
| Apert Syndrome |
|
Acrocephalosyndactyly Type I
|
Acs1
|
|
Acrocephalosyndactylia
|
Acs I
|
|
Apert-Crouzon Disease
|
Acrocephalosyndactyly
|
|
Acrocephalosyndactyly Type 1
|
Acrocephalosyndactyly, Type I
|
|
Acs 1
|
Acrocephalo-Syndactyly Type 1
|
|
Syndactylic Oxycephaly
|
Apert'S Syndrome
|
|
Type I Acrocephalosyndactyly
|
APRS
|
|
|
| Smoldering Myeloma |
|
|
| Childhood Absence Epilepsy |
|
Pyknolepsy
|
Petit Mal Epilepsy
|
|
Absence Seizures
|
Absence Seizure
|
|
Petit Mal Seizure
|
Absence Epilepsy, Childhood
|
|
Pykno-Epilepsy
|
Epilepsy, Absence
|
|
Absence Epilepsy
|
Pycnolepsy
|
|
|
| Jackson-Weiss Syndrome |
|
JWS
|
Craniosynostosis, Midfacial Hypoplasia, And Foot Abnormalities
|
|
Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities Syndrome
|
Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities
|
|
|
| Bladder Cancer |
|
Urinary Bladder Cancer
|
Bladder Carcinoma
|
|
Urinary Bladder Carcinoma
|
Bladder Neoplasm
|
|
Bladder Tumor
|
Cancer, Bladder
|
|
Malignant Neoplasm Of Urinary Bladder
|
Carcinoma Of Bladder
|
|
Bladder Cancer, Somatic
|
Tumor Of The Bladder
|
|
Carcinoma Of Urinary Bladder
|
Bladder Carcinoma Urinary
|
|
Cancer Of The Urinary Bladder
|
Cancer, Urinary Bladder
|
|
Malignant Bladder Neoplasm
|
Malignant Bladder Tumor
|
|
Neoplasm Of The Bladder
|
Neoplasm Of The Urinary Bladder
|
|
Tumor Of The Urinary Bladder
|
Urinary Bladder Neoplasm
|
|
BLC
|
Urothelial Carcinoma Of The Bladder
|
|
Bladder Tumors
|
Urinary Bladder Neoplasms
|
|
Bladder Cancer Nos
|
Vesical Cancer Nos
|
|
Malignant Neoplasm Of Bladder, Part Unspecified
|
Malignant Tumour Of Urinary Bladder
|
|
Primary Malignant Neoplasm Of Bladder
|
|
|
| Testicular Germ Cell Cancer |
|
Germ Cell Tumor Of Testis
|
Testicular Germ Cell Tumor
|
|
Testicular Germ Cell Neoplasm
|
Testicular Malignant Germ Cell Tumor
|
|
|
| Camptodactyly, Tall Stature, And Hearing Loss Syndrome |
|
|
| Fgfr3-Related Chondrodysplasia |
|
|
| Testicular Cancer |
|
Testis Cancer
|
Testicular Carcinoma
|
|
Testicular Neoplasms
|
Malignant Neoplasm Of Testis
|
|
Childhood Neoplasm Of The Testis
|
Neoplasm Of Testis
|
|
Pediatric Testicular Neoplasm
|
Testicular Tumor
|
|
Testis Neoplasm
|
Testicular Tumors
|
|
Testicular Neoplasm
|
Testicular Malignant Germ Cell Tumor
|
|
Childhood Testicular Neoplasm
|
Carcinoma Of The Testis
|
|
Cancer Of Testis
|
Malignant Neoplasm Of Testis, Nos
|
|
Malignant Neoplasm Of Testis, Unspecified
|
Malignant Tumour Of Testis
|
|
Testicle Cancer
|
Primary Malignant Neoplasm Of Testis
|
|
|
| Spondyloepimetaphyseal Dysplasia, Strudwick Type |
|
Spondylometaphyseal Dysplasia
|
Strudwick Syndrome
|
|
Dappled Metaphysis Syndrome
|
Semd, Strudwick Type
|
|
Spondylometaepiphyseal Dysplasia Congenita, Strudwick Type
|
Smed, Strudwick Type
|
|
Smd
|
Smed Strudwick Type
|
|
SEMDSTWK
|
Smed, Type I
|
|
Semdc
|
Smed Type 1
|
|
Spondyloepimetaphyseal Dysplasia Strudwick Type
|
Sed Strudwick
|
|
Spondyloepimetaphyseal Dysplasia Congenita, Strudwick Type
|
Smed Type I
|
|
Spondyloepiphyseal Dysplasia Congenita With Dappled Metaphyses
|
Dysplasia, Spondyloepimetaphyseal, Strudwick Type
|
|
Dysplasia, Spondylometaphyseal
|
|
|
| Crouzon Syndrome |
|
Crouzon Craniofacial Dysostosis
|
Craniofacial Dysostosis
|
|
Cfd1
|
Craniofacial Dysostosis Type 1
|
|
Crouzon Disease
|
Crouzon'S Disease
|
|
Craniofacial Dysostosis, Type I
|
Craniofacial Dysarthrosis
|
|
Craniofacial Dysostosis Syndrome
|
CS
|
|
Craniofacial Dysostosis Type I
|
Vogt Cephalosyndactyly
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Crouzon Syndrome With Acanthosis Nigricans |
|
Crouzon Syndrome-Acanthosis Nigricans Syndrome
|
CAN
|
|
Crouzonodermoskeletal Syndrome
|
Crouzon-Dermoskeletal Syndrome
|
|
Crouzon, With Acanthosis Nigricans Syndrome
|
|
|
| Leri-Weill Dyschondrosteosis |
|
LWD
|
Dyschondrosteosis
|
|
Dco
|
Léri-Weill Dyschondrosteosis
|
|
Leri Weill Dyschondrosteosis
|
Leri-Weill Syndrome
|
|
Leri-Weil Syndrome
|
Dyschondrosteosis, Leri-Weill
|
|
|
| Beare-Stevenson Cutis Gyrata Syndrome |
|
Cutis Gyrata Syndrome Of Beare And Stevenson
|
Beare-Stevenson Syndrome
|
|
BSTVS
|
Cutis Gyrata-Acanthosis Nigricans-Craniosynostosis Syndrome
|
|
Beare Stevenson Syndrome
|
Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis
|
|
Cutis Gyrata Syndrome Of Beare-Stevenson
|
|
|
| Brachydactyly |
|
|
| Cervix Carcinoma |
|
Cancer Of Cervix
|
Carcinoma Of Cervix
|
|
Carcinoma Cervix Uteri
|
Carcinoma Of The Cervix Uteri
|
|
|
| Osteogenesis Imperfecta, Type Ii |
|
Vrolik Type Of Osteogenesis Imperfecta
|
Osteogenesis Imperfecta Type 2
|
|
OI2
|
Oi, Type Ii
|
|
Osteogenesis Imperfecta Congenita
|
Oic
|
|
Osteogenesis Imperfecta Type Ii
|
Lethal Osteogenesis Imperfecta
|
|
Oi Type 2
|
Osteogenesis Imperfecta Congenita Perinatal Lethal Form
|
|
Osteogenesis Imperfecta Congenita, Perinatal Lethal Form
|
Perinatal Lethal Osteogenesis Imperfecta Congenita
|
|
Perinatally Lethal Oi
|
Osteogenesis Imperfecta 2
|
|
Oi-Ii
|
Oi-Iia
|
|
Oi Type Iia
|
Osteogenesis Imperfecta Type Iia
|
|
Osteogenesis Imperfecta Type Ii Autosomal Dominant
|
Oi Type Ii
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
|
|
| Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome |
|
Catshl Syndrome
|
Camptodactyly-Tall Stature-Scoliosis-Deafness Syndrome
|
|
|
| Spondyloepiphyseal Dysplasia Congenita |
|
SEDC
|
Sed Congenita
|
|
Spondyloepiphyseal Dysplasia, Congenital Type
|
Late Spondyloepiphyseal Dysplasia
|
|
Sed, Congenital Type
|
Congenital Spondyloepiphyseal Dysplasia
|
|
Spranger-Wiedemann Disease
|
Spondyloepiphyseal Dysplasia Congenital Type
|
|
Dysplasia, Spondyloepiphyseal, Congenita
|
Spondyloepiphyseal Dysplasia, Congenita
|
|
Spondyloepiphyseal Dysplasia Tarda, X-Linked
|
|
|
| Noonan Syndrome 1 |
|
Noonan Syndrome
|
NS1
|
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
| Hypertelorism, Microtia, Facial Clefting Syndrome |
|
Hmc Syndrome
|
Bixler Christian Gorlin Syndrome
|
|
Bixler-Christian-Gorlin Syndrome
|
Hypertelorism-Microtia-Facial Clefting Syndrome
|
|
Bixler Syndrome
|
Hypertelorism-Microtia-Clefting Syndrome
|
|
Hypertelorism Microtia Facial Clefting Syndrome
|
|
|
| Brittle Bone Disorder |
|
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
|
Fragilitas Ossium
|
Osteopsathyrosis
|
|
Lobstein Disease
|
Oi
|
|
Vrolik Disease
|
Lobstein'S Disease
|
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
|
Porak And Durante Disease
|
Glass Bone Disease
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
|
Ossium Fragility
|
Osteitis Fragilitans
|
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
| Teratoma |
|
|
| Gliosarcoma |
|
Glioblastoma With Sarcomatous Component
|
Sarcomatous Glioblastoma
|
|
|
| Ureteral Benign Neoplasm |
|
Neoplasm Of Ureter
|
Ureteral Tumor
|
|
Cancer Of The Ureter
|
Malignant Tumour Of Ureter
|
|
Ureteric Cancer
|
Primary Malignant Neoplasm Of Ureter
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Acromesomelic Dysplasia |
|
Acromesomelic Dwarfism
|
Dysplasia, Acromesomelic
|
|
Acromesomelic Dysplasia Hunter-Thompson Type
|
|
|
| Luteoma |
|
Leuteoma Of Pregnancy
|
Luteoma Of Pregnancy
|
|
|
| Myeloma, Multiple |
|
Multiple Myeloma
|
Kahler Disease
|
|
Myelomatosis
|
Plasma Cell Myeloma
|
|
Medullary Plasmacytoma
|
Multiple Myeloma, Resistance To
|
|
Myeloma
|
Plasma Cell Dyscrasia
|
|
Multiple Myeloma, Susceptibility To
|
Myeloma - Multiple
|
|
Kahler'S Disease
|
Kahler-Bozzolo Disease
|
|
Plasma Cell Myelomas
|
MM
|
|
Plasma Cell Neoplasm
|
Primary Systemic Amyloidosis
|
|
Primary Amyloidosis
|
Immunoglobulin Deposition Disease
|
|
Plasmacytic Myeloma
|
Multiple Myelomata
|
|
Multiple Myeloma Nos
|
Multiple Myeloma Without Mention Of Remission
|
|
Monostotic Plasma Cell Myeloma
|
Mm - [Multiple Myeloma]
|
|
|
| Cutaneous Ganglioneuroma |
|
|
| Enchondromatosis, Multiple, Ollier Type |
|
Ollier Disease
|
Enchondromatosis
|
|
Dyschondroplasia
|
Osteochondromatosis
|
|
Multiple Cartilaginous Enchondroses
|
Multiple Enchondromatosis
|
|
Enchondromatosis With Haemangiomata
|
Enchondromatosis, Multiple
|
|
Kast'S Syndrome
|
Ollier'S Syndrome
|
|
Enchondromatosis Multiple
|
ENCHOM
|
|
Maffucci Disease
|
Olliers Disease
|
|
Hereditary Multiple Exostoses
|
Chondromatosis
|
|
|
| Polyhydramnios |
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Breast Cancer, Familial
|
|
Malignant Neoplasm Of Breast
|
Male Breast Cancer
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Hypochondroplasia |
|
HCH
|
Hypochondrodysplasia
|
|
Chondrogenesis Imperfecta
|
Hypochondroplastic Dwarfism
|
|
Hypochondroplastic Short Stature
|
|
|
| Rhabdomyosarcoma |
|
|
| Keratosis |
|
Actinic Keratosis
|
Hyperkeratosis
|
|
|
| Plasma Cell Neoplasm |
|
Plasma Cell Dyscrasia
|
Paraproteinemias
|
|
Plasma Cell Tumour
|
Plasmacytic Tumor
|
|
Multiple Myeloma
|
Plasmacytoma
|
|
Plasma Cell Tumours
|
Plasma Cells Dyscrasia
|
|
|
| Ectodermal Dysplasia |
|
Congenital Ectodermal Defect
|
Congenital Ectodermal Dysplasia
|
|
Ectodermal Dysplasia Syndrome
|
Dysplasia, Ectodermal
|
|
|
| Non-Syndromic Bicoronal Craniosynostosis |
|
Isolated Bicoronal Craniosynostosis
|
Isolated Brachycephaly
|
|
Non-Syndromic Bilateral Coronal Suture Synostosis
|
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Lynch Syndrome |
|
Hereditary Nonpolyposis Colon Cancer
|
Hereditary Nonpolyposis Colorectal Cancer
|
|
Hereditary Nonpolyposis Colorectal Carcinoma
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
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Familial Nonpolyposis Colon Cancer
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Hnpcc
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Coca 1
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Hereditary Defective Mismatch Repair Syndrome
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Hereditary Non-Polyposis Colon Cancer
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Hereditary Non-Polyposis Colon Cancer Syndrome
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Hereditary Non-Polyposis Colorectal Cancer
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Hereditary Non-Polyposis Colorectal Cancer Syndrome
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Hereditary Nonpolyposis Colon Cancer Syndrome
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Hereditary Nonpolyposis Colorectal Cancer Syndrome
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Hereditary Nonpolyposis Colorectal Neoplasm
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Hnpcc - Hereditary Nonpolyposis Colon Cancer
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Cancer Family Syndrome
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Familial Nonpolyposis Colorectal Cancer
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Colon Cancer, Familial Nonpolyposis
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Colorectal Neoplasms, Hereditary Nonpolyposis
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Cancer, Colorectal, Nonpolyposis, Hereditary
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Colorectal Cancer, Hereditary Nonpolyposis, Type 1
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| Lung Squamous Cell Carcinoma |
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Squamous Cell Carcinoma Of Lung
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Squamous Cell Lung Carcinoma
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Epidermoid Cell Carcinoma Of The Lung
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Squamous Cell Lung Cancer
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| Lacrimoauriculodentodigital Syndrome |
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Ladd Syndrome
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Levy-Hollister Syndrome
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Lacrimo-Auriculo-Dento-Digital Syndrome
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LADD
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Lacrimoauriculodento-Digital Syndrome
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Levy Hollister Syndrome
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Lard Syndrome
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Lacrimoauriculoradiodental Syndrome
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LADDS
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Congenital Duodenal Obstruction Due To Malrotation Of Intestine
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| Carpenter Syndrome 1 |
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Carpenter Syndrome
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Acrocephalopolysyndactyly Type Ii
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Acps Ii
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CRPT1
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Acrocephalopolysyndactyly Type 2
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Acrocephalosyndactyly, Type Ii
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Acrocephalopolysyndactyly 2
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Acps2
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Acps 2
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Type Ii Acrocephalosyndactyly
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Carpenter Syndrome, Type 1
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Apert-Crouzon Disease
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| Proteus Syndrome |
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Proteus Syndrome, Somatic
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Partial Gigantism-Nevi-Hemihypertrophy-Macrocephaly Syndrome
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Gigantism, Partial, Of Hands And Feet, Nevi, Hemihypertrophy, And Macrocephaly
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Wiedemann'S Syndrome
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Hemihypertrophy And Macrocephaly
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Partial Gigantism Of Hands And Feet, Nevi, Hemihypertrophy, Macrocephaly
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Ps
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PROTEUSS
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Partial Gigantism Of Hands And Feet Nevi Hemihypertrophy And Macrocephaly
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| Osteochondrodysplasia |
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Chondrodystrophy
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Skeletal Dysplasia
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Congenital Anomaly Of Cartilage
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Osteochondrodysplasias
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Cartilage Development Disorder
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Osteochondrodysplasia Syndrome
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Dysplasia, Skeletal
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Mucopolysaccharidosis Iv
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| Peripheral T-Cell Lymphoma |
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Lymphoma T-Cell Peripheral
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| Parietal Foramina |
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Enlarged Parietal Foramina
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Hereditary Cranium Bifidum
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Symmetric Parietal Foramina
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Catlin Marks
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Foramina Parietalia Permagna
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Caitlin Marks
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Cranium Bifidum
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Cranium Bifidum Occultum
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Fenestrae Parietals Symmetricae
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Fpp
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Giant Parietal Foramina
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Pfm
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Fenestrae Parietales Symmetricae
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Foramina, Parietal
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| Bone Disease |
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Bone Diseases
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Skeletal Disease
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Skeletal Disorder
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Disorder Of Skeletal System
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| Huntington Disease |
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Huntington'S Disease
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Huntington Chorea
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HD
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Huntington'S Chorea
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Huntington Chronic Progressive Hereditary Chorea
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Juvenile Huntington Disease
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Chronic Progressive Chorea
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Chronic Progressive Hereditary Chorea
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Hc - [Huntington Chorea]
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Hereditary Chorea
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Progressive Hereditary Chorea
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| Myeloproliferative Neoplasm |
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Myeloproliferative Disorder
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Chronic Myeloproliferative Disease
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Myeloproliferative Neoplasms
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Chronic Myeloproliferative Disorder
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Cmpd
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Cmpd, U
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Chronic Myeloproliferative Disorders
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Mpd
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Mpn
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Myeloproliferative Disorders
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Myeloproliferative Disease
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Campomelic Dysplasia
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| Chondroblastoma |
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| Gastric Cancer |
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Stomach Cancer
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Stomach Carcinoma
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Gastric Carcinoma
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Gastric Cancer, Somatic
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Gastric Neoplasm
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Carcinoma Of Stomach
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Stomach Neoplasms
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Malignant Neoplasm Of Stomach
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Gastric Cancer Risk After H. Pylori Infection
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Cancer Of The Stomach
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Adult Stomach Cancer
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Adult Stomach Carcinoma
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GASC
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Gastric Cancer Intestinal
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Gastric Cancers
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Gastric Carcinomas
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Cancer, Gastric
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Stomach Neoplasm
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Malignant Neoplasm Of Body Of Stomach
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Malignant Tumor Of Lesser Curve Of Stomach
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Gastrocarcinoma Of Unspecified Site
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Leather Bottle Stomach
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Carcinoma Of Fundus Of Stomach
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Cancer Of Fundus Of Stomach
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Primary Malignant Neoplasm Of Body Of Stomach
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Cancer Of Body Of Stomach
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Primary Malignant Neoplasm Of Pyloric Antrum
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Pyloric Antrum Cancer
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Malignant Tumour Of Stomach
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| Breast Juvenile Papillomatosis |
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Juvenile Papillomatosis Of The Breast
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| Dysostosis |
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| Cleft Palate, Isolated |
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Cleft Palate
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Isolated Cleft Palate
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CPI
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Cp
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Palatoschisis
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Cleft Palate Isolated
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Uranostaphyloschisis
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Congenital Fissure Of Palate
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Cleft Of Secondary Palate
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| Melanoacanthoma |
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| Orofacial Cleft |
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| Dowling-Degos Disease 1 |
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Reticular Pigment Anomaly Of Flexures
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DDD1
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Ddd
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Dowling-Degos Disease
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Hyperpigmentation
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| Holoprosencephaly |
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Holoprosencephaly Sequence
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Hpe
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Hpe - [Holoprosencephaly]
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| Saethre-Chotzen Syndrome |
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SCS
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Acs3
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Acs Iii
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Chotzen Syndrome
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Acrocephaly, Skull Asymmetry, And Mild Syndactyly
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Acrocephalosyndactyly Type 3
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Acrocephalosyndactyly, Type Iii
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Acrocephalosyndactyly Type Iii
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Saethre-Chotzen Syndrome With Or Without Eyelid Anomalies
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Auralcephalosyndactyly
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Acs 3
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Acrocephalo-Syndactyly, Type 3
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Blepharophimosis,Epicanthus Inversus, And Ptosis 3
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Aural Cephalosyndactyly
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Kurczynski-Casperson Syndrome
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Acrocephalosyndactyly Iii
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Dysostosis Craniofacialis With Hypertelorism
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Saethre-Chotzen Syndrome, With/Without Eyelid Anomalies
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Sakati Syndrome
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| Synostosis |
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