| Diseases |
Alias |
|
| Breast Medullary Carcinoma |
|
Medullary Breast Carcinoma
|
Medullary Breast Carcinoma With Lymphoid Stroma
|
|
Medullary Carcinoma Of Breast
|
|
|
| Coloboma, Ocular, With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation |
|
Uveal Coloboma-Cleft Lip And Palate-Intellectual Disability
|
COB1
|
|
Coloboma-Microphthalmos Syndrome
|
Coloboma-Microphthalmos Syndrome Associated With Sensorineural Hearing Loss, Hematuria, And Cleft Lip/Palate
|
|
Coloboma, Cleft Lip-Palate And Mental Retardation Syndrome
|
Ocular Coloboma With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation
|
|
Uveal Coloboma-Cleft Lip/Palate-Mental Retardation Syndrome
|
Uveal Coloboma-Cleft Lip/Palate-Intellectual Disability Syndrome
|
|
Coloboma, Ocular, With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Intellectual Disability
|
Coloboma, Ocular, With/Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation
|
|
|
| Adjustment Disorder |
|
Adjustment Reaction
|
Adjustment Disorders
|
|
Adjustment Disease
|
Brief Situational Non-Psychotic Disorder
|
|
Adaptation Reaction Nos
|
Emotional Crisis
|
|
Situational Disorder
|
Situational Disturbance
|
|
Situational Maladjustment
|
Situational Reaction
|
|
Situational Reaction With Maladjustment
|
Transient Situational Disturbance
|
|
|
| Uterus Carcinoma In Situ |
|
|
| Cerebellar Ataxia Type 48 |
|
|
| Epilepsy, Familial Temporal Lobe, 3 |
|
Epilepsy, Familial Mesial Temporal Lobe
|
Fmtle
|
|
Familial Temporal Lobe Epilepsy 3
|
ETL3
|
|
Familial Mesial Temporal Lobe Epilepsy
|
|
|
| Germ Cell And Embryonal Cancer |
|
Germ Cell And Embryonal Neoplasm
|
|
|
| Cervix Uteri Carcinoma In Situ |
|
Carcinoma In Situ Of Cervix
|
Carcinoma In Situ Of Uterine Cervix
|
|
Cervical Intraepithelial Neoplasia
|
Carcinoma Of Cervix Stage 0
|
|
Cervical Intraepithelial Neoplasia Grade Iii With Severe Dysplasia
|
Cervix Ca In Situ
|
|
Cin Iii
|
Cin Iii - Carcinoma In Situ Of Cervix
|
|
Cin Iii - Severe Dyskaryosis
|
Severe Dysplasia Of Cervix
|
|
Severe Dysplasia Of The Cervix Uteri
|
Squamous Intraepithelial Neoplasia, Grade Iii
|
|
Cervix Intraepithelial Neoplasia Grade 3 Ajcc V7
|
|
|
| Dysembryoplastic Neuroepithelial Tumor |
|
Dysembryoplastic Neuroepithelial Tumour
|
Dysembryoplastic Neuroepithelial Neoplasm
|
|
Dnet
|
|
|
| Atrichia With Papular Lesions |
|
Papular Atrichia
|
APL
|
|
Congenital Atrichia
|
|
|
| Benign Breast Phyllodes Tumor |
|
Phyllodes Tumor
|
Benign Cystosarcoma Phyllodes
|
|
Benign Phyllodes Neoplasm
|
Benign Phyllodes Neoplasm Of The Breast
|
|
Cystosarcoma Phyllodes
|
Phyllodes Neoplasm
|
|
Phyllodes Tumor, Benign
|
|
|
| Myiasis |
|
Infestation By Fly Larvae
|
Infestation By Maggots
|
|
Maggot Infestation
|
Infestation By Larvae Of Flies
|
|
Infestation By Dermatobia
|
Infestation By Estrus Ovis
|
|
Infestation By Oestrus Ovis
|
Oestriasis
|
|
Oestrosis
|
|
|
| Comedo Carcinoma |
|
Comedocarcinoma
|
High Grade Ductal Breast Carcinoma In Situ
|
|
|
| Postpoliomyelitis Syndrome |
|
Postpolio Syndrome
|
Post-Polio Syndrome
|
|
Post Polio Syndrome
|
Polio Late Effects
|
|
Post-Polio Muscular Atrophy
|
Post-Polio Sequelae
|
|
Post-Poliomyelitic Syndrome
|
Postpolio Sequelae
|
|
Postpoliomyelitic Syndrome
|
Postpoliomyelitis Sequelae
|
|
|
| Chromosome 15q24 Deletion Syndrome |
|
15q24 Microdeletion Syndrome
|
Del(15)(Q24)
|
|
Monosomy 15q24
|
15q24 Microdeletion
|
|
15q24 Deletion
|
Interstitial Deletion Of Chromosome 15q24
|
|
|
| Teeth Hard Tissue Disease |
|
|
| Spinal Muscular Atrophy, Type Iv |
|
SMA4
|
Spinal Muscular Atrophy, Adult Form
|
|
Spinal Muscular Atrophy 4
|
Spinal Muscular Atrophy-4
|
|
Adult Spinal Muscular Atrophy
|
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Recessive
|
|
Proximal Spinal Muscular Atrophy Type 4
|
Sma Type 4
|
|
Sma Type Iv
|
Sma-Iv
|
|
Sma Iv
|
Spinal Muscular Atrophy Adult Form
|
|
Spinal Muscular Atrophy Proximal Adult Autosomal Recessive
|
Spinal Muscular Atrophy Type Iv
|
|
Atrophy, Muscular, Spinal, Type Iv
|
Myelopathic Muscular Atrophy
|
|
|
| Amelogenesis Imperfecta, Type Ig |
|
Enamel-Renal Syndrome
|
Ers
|
|
Amelogenesis Imperfecta Type 1g
|
AI1G
|
|
Enamel-Renal-Gingival Syndrome
|
Amelogenesis Imperfecta And Gingival Fibromatosis Syndrome
|
|
Aigfs
|
Amelogenesis Imperfecta, Hypoplastic, With Nephrocalcinosis
|
|
Amelogenesis Imperfecta Hypoplastic With Nephrocalcinosis
|
Amelogenesis Imperfecta Type Ig
|
|
Amelogenesis Imperfecta-Nephrocalcinosis Syndrome
|
Amelogenesis Imperfecta 1g
|
|
Hypoplastic Amelogenesis Imperfecta With Nephrocalcinosis
|
Amelogenesis Imperfecta Nephrocalcinosis
|
|
|
| 46,Xy Sex Reversal 2 |
|
Dosage-Sensitive Sex Reversal
|
Dss
|
|
SRXY2
|
46,Xy Sex Reversal, Dax1-Related
|
|
46xy Sex Reversal 2, Dosage-Sensitive
|
46,Xy Sex Reversal Dax1-Related
|
|
|
| Anus Benign Neoplasm |
|
Anal Neoplasm
|
Anal Tumors
|
|
Neoplasm Of Anus
|
Anus Neoplasms
|
|
|
| Laryngomalacia |
|
Congenital Laryngomalacia
|
Congenital Laryngeal Stridor
|
|
Laryngomalacia Congenital
|
Floppy Epiglottis
|
|
|
| Weaver Syndrome |
|
Wss
|
Weaver-Smith Syndrome
|
|
WVS
|
Weaver-Like Syndrome
|
|
Weaver-Williams Syndrome
|
Camptodactyly-Overgrowth-Unusual Facies Syndrome
|
|
Camptodactyly - Overgrowth - Unusual Facies
|
Ezh2 Related Overgrowth
|
|
Overgrowth Syndrome With Accelerated Skeletal Maturation, Unusual Facies, And Camptodactyly
|
Weaver Smith Syndrome
|
|
Weaver Like Syndrome
|
Weaver Williams Syndrome
|
|
Camptodactyly-Overgrowth-Unusual Facies
|
Weaver Syndrome 1
|
|
Weaver Syndrome 2
|
Wvs1
|
|
Wvs2
|
|
|
| Hypoparathyroidism-Retardation-Dysmorphism Syndrome |
|
Sanjad-Sakati Syndrome
|
Hrd Syndrome
|
|
HRDS
|
Hypoparathyroidism-Intellectual Disability-Dysmorphism Syndrome
|
|
Hypoparathyroidism-Short Stature-Intellectual Disability-Seizures Syndrome
|
Richardson-Kirk Syndrome
|
|
Sss
|
Hypoparathyroidism With Short Stature, Mental Retardation, And Seizures
|
|
Hypoparathyroidism, Congenital, Associated With Dysmorphism, Growth Retardation, And Developmental Delay
|
Hypoparathyroidism With Short Stature, Mental Retardation And Seizures
|
|
Hypoparathyroidism With Short Stature, Intellectual Disability And Seizures
|
Hypoparathyroidism, Congenital, Associated With Dysmorphism, Growth Retardation And Developmental Delay
|
|
|
| Germ Cell Cancer |
|
Malignant Germ Cell Tumor
|
Neoplasms, Germ Cell And Embryonal
|
|
Germ Cell Neoplasm
|
Germ Cell Tumour
|
|
Malignant Tumor Of The Germ Cell
|
Neoplasms Germ Cell
|
|
Malignant Germ Cell Neoplasm
|
|
|
| Filarial Elephantiasis |
|
Lymphatic Filariasis
|
Elephantiasis
|
|
Filariasis
|
Bancroftian Elephantiasis
|
|
Bancroftian Filarial Chyluria
|
Elephantiasis Of Eyelid
|
|
Bancroftian Filariasis
|
Elephantitis
|
|
Malayi Tropical Eosinphilia
|
Wuchereria Bancrofti Infection
|
|
Wuchereriasis
|
Elephantiasis, Filarial
|
|
Filarial Elephantiases
|
Infection By Wuchereria Bancrofti
|
|
Filarial Lymphangitis
|
Tropical Elephantiasis
|
|
Filarial Chylocele
|
|
|
| Microphthalmia, Syndromic 9 |
|
Matthew-Wood Syndrome
|
Spear Syndrome
|
|
Anophthalmia/Microphthalmia And Pulmonary Hypoplasia
|
Microphthalmia, Isolated, With Coloboma 8
|
|
MCOPS9
|
Anophthalmia, Clinical, With Mild Facial Dysmorphism And Variable Malformations Of The Lung, Heart, And Diaphragm
|
|
Pulmonary Hypoplasia-Diaphragmatic Hernia-Anophthalmia-Cardiac Defect
|
Pdac
|
|
Pulmonary Agenesis, Microphthalmia, And Diaphragmatic Defect
|
Pmd
|
|
Syndromic Microphthalmia 9
|
Anophthalmia-Pulmonary Hypoplasia Syndrome
|
|
Clinical Anophthalmia Mild Facial Dysmorphism Lung Heart And Diaphragm Malformations
|
Pulmonary Agenesis Microphthalmi And Diaphragmatic Defect
|
|
Microphthalmia Syndromic 9
|
Matthew Wood Syndrome
|
|
Pdac Syndrome
|
Pulmonary Hypoplasia-Diaphragmatic Hernia-Anophthalmia-Cardiac Defect Syndrome
|
|
Microphthalmia, Isolated, With Coloboma, 8
|
MCOPCB8
|
|
Isolated Colobomatous Microphthalmia 8
|
Microphthalmia, Syndromic, 9
|
|
Anophthalmia With Pulmonary Hypoplasia
|
Microphthalmia Syndromic, Type 9
|
|
Anophthalmia And Pulmonary Hypoplasia
|
|
|
| Thyroid Hormone Resistance, Generalized, Autosomal Dominant |
|
Thyroid Hormone Resistance Syndrome
|
Thyroid Hormone Resistance
|
|
GRTHD
|
Gthr
|
|
Thyroid Hormone Unresponsiveness
|
Generalized Thyroid Hormone Resistance
|
|
Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Thyroid Hormones
|
Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones
|
|
Refetoff Syndrome
|
Thyroid Hormone Responsiveness Defect
|
|
Familial Euthyroid Hyperthyroxinemia, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones
|
Thyroid Hormone Resistance, Generalized, Autosomal Recessive
|
|
|
| Bruxism |
|
Sleep Bruxism
|
Sleep-Related Bruxism
|
|
Bruxism - Teeth Grinding
|
Grinding Teeth
|
|
Sleep Related Bruxism
|
Teeth Grinding
|
|
Sleep Related Teeth Grinding
|
|
|
| Larsen Syndrome |
|
LRS
|
Larsen Syndrome, Dominant Type
|
|
Dominant Larsen Syndrome
|
Autosomal Dominant Larsen Syndrome
|
|
Larsens Syndrome
|
|
|
| 46,Xy Sex Reversal |
|
Swyer Syndrome
|
Pure Gonadal Dysgenesis 46,Xy
|
|
Gonadal Dysgenesis, Xy Female Type
|
Gonadal Dysgenesis, 46,Xy
|
|
46,Xy Cgd
|
46,Xy Complete Gonadal Dysgenesis
|
|
46,Xy Pure Gonadal Dysgenesis
|
46 Xy Gonadal Dysgenesis
|
|
46, Xy Cgd
|
46, Xy Complete Gonadal Dysgenesis
|
|
46, Xy Pure Gonadal Dysgenesis
|
Xy Pure Gonadal Dysgenesis
|
|
Female With 46,Xy Karyotype
|
Xy Females
|
|
|
| Epilepsy, Familial Temporal Lobe, 1 |
|
ETL1
|
Adpeaf
|
|
Adlte
|
Epilepsy, Partial, With Auditory Features
|
|
Autosomal Dominant Partial Epilepsy With Auditory Features
|
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant
|
|
Familial Temporal Lobe Epilepsy 1
|
Partial Epilepsy With Auditory Features
|
|
Autosomal Dominant Lateral Temporal Lobe Epilepsy
|
Lateral Temporal Lobe Epilepsy Autosomal Dominant
|
|
Epilepsy, Temporal Lobe, Familial, Type 1
|
|
|
| Postpartum Depression |
|
Maternity Blues
|
Postnatal Depression
|
|
Depression, Postpartum
|
Post-Partum Depression
|
|
Depression Postpartum
|
|
|
| Amelogenesis Imperfecta |
|
Ai
|
Congenital Enamel Hypoplasia
|
|
Al - [Amelogenesis Imperfecta]
|
|
|
| Phelan-Mcdermid Syndrome |
|
Chromosome 22q13.3 Deletion Syndrome
|
22q13.3 Deletion Syndrome
|
|
Telomeric 22q13 Monosomy Syndrome
|
PHMDS
|
|
Deletion 22q13 Syndrome
|
22q13.3 Deletion
|
|
Deletion 22q13.3 Syndrome
|
Monosomy 22q13
|
|
Monosomy 22q13.3
|
22q13 Deletion Syndrome
|
|
Monosomy 22q13 Syndrome
|
22q13 Deletion
|
|
Chromosome Deletion
|
|
|
| Hyperoxaluria, Primary, Type I |
|
Primary Hyperoxaluria Type 1
|
HP1
|
|
Glycolic Aciduria
|
Alanine-Glyoxylate Aminotransferase Deficiency
|
|
Hepatic Agt Deficiency
|
Oxalosis I
|
|
Primary Hyperoxaluria, Type I
|
Serine:Pyruvate Aminotransferase Deficiency
|
|
Hyperoxaluria, Primary, Type 1
|
Peroxisomal Alanine-Glyoxylate Aminotransferase Deficiency
|
|
Peroxisomal Alanine Glyoxylate Aminotransferase Deficiency
|
Serine Pyruvate Aminotransferase Deficiency
|
|
Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency
|
Oxalosis 1
|
|
Hyperoxaluria Primary 1
|
Hyperoxaluria Primary Type I
|
|
Ph1
|
Primary Hyperoxaluria Type I
|
|
Oxalosis Type 1
|
2-Oxoglutarate Glyoxylate Carboligase Deficiency
|
|
|
| Central Nervous System Lymphoma |
|
Microglioma
|
Primary Cns Lymphoma
|
|
Cns Lymphoma
|
Primary Central Nervous System Lymphoma
|
|
|
| Endometrial Stromal Tumor |
|
Endometrial Stromal Neoplasm
|
Endometrial Stromal Tumors
|
|
|
| Central Nervous System Hematologic Cancer |
|
Cns Hematopoietic Tumor
|
Hematopoietic Neoplasm Of Central Nervous System
|
|
Central Nervous System Hematopoietic Neoplasm
|
|
|
| Primary Hyperoxaluria |
|
Hyperoxaluria
|
Hyperoxaluria, Primary
|
|
Oxalosis
|
Primary Oxalosis
|
|
Congenital Oxaluria
|
D-Glycerate Dehydrogenase Deficiency
|
|
Glyceric Aciduria
|
Glycolic Aciduria
|
|
Hepatic Agt Deficiency
|
Oxaluria, Primary
|
|
Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency
|
Primary Oxaluria
|
|
Hyperoxaluria Primary
|
Primary Hyperoxaluria Type 2
|
|
Primary Hyperoxaluria, Type I
|
|
|
| Breast Adenocarcinoma |
|
Mammary Adenocarcinoma
|
Adenocarcinoma Of Breast
|
|
|
| Endometrial Stromal Sarcoma |
|
Ess
|
Endometrial Stromal Sarcoma, High Grade
|
|
Undifferentiated Endometrial Sarcoma
|
Stromal Sarcoma Of The Corpus Uteri
|
|
Sarcoma Endometrial Stromal
|
Sarcoma, Endometrial Stromal
|
|
Undifferentiated Stromal Sarcoma
|
|
|
| Diamond-Blackfan Anemia |
|
Congenital Pure Red Cell Aplasia
|
Aase Syndrome
|
|
Erythrogenesis Imperfecta
|
Anemia, Diamond-Blackfan
|
|
Congenital Hypoplastic Anemia
|
Aase-Smith Ii Syndrome
|
|
Bds
|
Blackfan-Diamond Anemia
|
|
Congenital Prca
|
Congenital Hypoplastic Anemia, Blackfan-Diamond Type
|
|
Dba
|
Blackfan - Diamond Syndrome
|
|
Chronic Constitutional Pure Red Cell Anaemia
|
Anemia Diamond Blackfan Type
|
|
Anemia Congenital Erythroid Hypoplastic
|
Aregenerative Anemia Chronic Congenital
|
|
Blackfan Diamond Syndrome
|
Red Cell Aplasia, Pure Hereditary
|
|
Aase-Smith Syndrome Ii
|
Bda
|
|
Blackfan Diamond Anemia
|
Blackfan-Diamond Disease
|
|
Blackfan-Diamond Syndrome
|
Chronic Congenital Agenerative Anemia
|
|
Congenital Erythroid Hypoplastic Anemia
|
Congenital Hypoplastic Anemia Of Blackfan And Diamond
|
|
Congenital Pure Red Cell Anemia
|
Hypoplastic Congenital Anemia
|
|
Inherited Erythroblastopenia
|
Pure Hereditary Red Cell Aplasia
|
|
Anemia, Hypoplastic, Congenital
|
Anemia Hypoplastic Congenital
|
|
Fanconi Anemia
|
Constitutional Aplastic Anemia
|
|
Diamond-Blackfan Anemia 1
|
Aase Smith Syndrome 2
|
|
Congenital Red Cell Aplasia
|
Red Cell Aplasia Of Infants
|
|
Pure Red Cell Aplasia Of Infants
|
Congenital Red Cell Aplastic Anaemia
|
|
Congenital Pure Red Cell Anaemia
|
Congenital Erythroid Hypoplasia
|
|
Pearson Marrow-Pancreas Syndrome
|
|
|
| Retinal Cancer |
|
Malignant Neoplasm Of Retina
|
Retinal Neoplasms
|
|
Malignant Retinal Neoplasm
|
Malignant Tumor Of Retina
|
|
Neoplasm Of Retina
|
Retinal Tumor
|
|
Retinal Neoplasm
|
Cancer Of The Retina
|
|
Malignant Retinal Tumour
|
Malignant Tumour Of Retina
|
|
Primary Malignant Neoplasm Of Retina
|
|
|
| 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
|
|
|
| Male Reproductive Organ Cancer |
|
Genital Neoplasms, Male
|
Male Genital Cancer
|
|
Male Genital Neoplasm
|
Male Reproductive System Neoplasm
|
|
Malignant Neoplasm Of Male Genital Organ
|
Malignant Neoplasm Of Male Genital Organ Or Tract
|
|
Malignant Neoplasm Of Male Genital Organs
|
Malignant Tumor Of Male Genital Organ
|
|
Malignant Tumor Of Male Reproductive System
|
Neoplasm Of Male Genital Organ
|
|
Tumor Of Male Reproductive System
|
|
|
| Diffuse Midline Glioma, H3 K27m-Mutant |
|
Diffuse Intrinsic Pontine Glioma
|
Dipg
|
|
Infiltrative Brainstem Glioma
|
|
|
| Thoracic Cancer |
|
Thoracic Tumor
|
Thorax Cancer
|
|
Thorax Neoplasm
|
Tumor Of Thorax
|
|
Thoracic Neoplasms
|
|
|
| Retinal Disease |
|
Retinal Diseases
|
Retinal Disorder
|
|
Retinal Disorders
|
|
|
| Sensory System Disease |
|
|
| Chromosomal Deletion Syndrome |
|
|
| Leukemia, Acute Myeloid |
|
Acute Myeloid Leukemia
|
Leukemia, Acute Myelogenous
|
|
Acute Myelogenous Leukemia
|
AML
|
|
Leukemia, Acute Myeloid, Susceptibility To
|
Acute Myeloblastic Leukemia
|
|
Leukemia, Acute Myeloid, Reduced Survival In, Somatic
|
Acute Myeloid Leukaemia
|
|
Leukemia, Myelocytic, Acute
|
Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
|
|
Secondary Aml
|
Acute Myelocytic Leukemia
|
|
Acute Myeloid Leukemia, Somatic
|
Leukemia, Acute Myeloid, Somatic
|
|
Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic
|
Acute Myeloblastic Leukaemia
|
|
Acute Myelogenous Leukaemia
|
Aml - Acute Myeloid Leukemia
|
|
Acute Myeloid Leukemia With Cebpa Somatic Mutations
|
Aml With Cebpa Somatic Mutations
|
|
Inherited Acute Myeloid Leukemia
|
Familial Aml
|
|
Inherited Aml
|
Pure Familial Aml
|
|
Pure Familial Acute Myeloid Leukemia
|
Secondary Acute Myeloid Leukemia
|
|
Therapy-Related Aml And Myelodysplastic Syndrome
|
Acute Myeloid Leukemia, Secondary
|
|
Acute Non-Lymphoblastic Leukemia
|
Acute Non-Lymphocytic Leukemia
|
|
Acute Biphenotypic Leukemia
|
Acute Undifferentiated Leukemia
|
|
Acute Myeloblastic Leukaemia With Multilineage Dysplasia
|
Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission
|
|
Acute Myeloid Leukaemia With Myelodysplasia-Related Features
|
|
|
| Retinitis Pigmentosa 11 |
|
RP11
|
Retinitis Pigmentosa-11
|
|
Retinitis Pigmentosa, Type 11
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Acute Promyelocytic Leukemia |
|
Leukemia, Acute Promyelocytic
|
Acute Myeloblastic Leukemia Type 3
|
|
Aml M3
|
APL
|
|
Leukemia, Acute Promyelocytic, Somatic
|
Aml With T(15
|
|
17)(Q22
|
Q12)
|
|
(Pml/Raralpha) And Variants
|
Apml
|
|
Acute Myeloblastic Leukemia 3
|
Acute Myeloid Leukemia With T(15
|
|
17)(Q22
|
Q12)
|
|
(Pml/Raralpha) And Variants
|
Acute Myeloblastic Leukaemia Type 3
|
|
Acute Myeloid Leukaemia M3
|
Acute Myeloid Leukemia M3
|
|
Acute Promyelocytic Leukaemia
|
M3 Anll
|
|
Myeloid Leukemia, Acute, M3
|
Leukemia Promyelocytic Acute
|
|
Leukemia, Promyelocytic, Acute
|
Leukemia, Acute, Promyelocytic
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
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Peripheral Nerve Disease
|
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Peripheral Nerve Disorders
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Neuropathy, Peripheral
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Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
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| Nervous System Disease |
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Abnormality Of The Nervous System
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Nervous System Diseases
|
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Nervous System Disorder
|
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| Connective Tissue Disease |
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Connective Tissue Diseases
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Connective Tissue Disorder
|
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Abnormality Of Connective Tissue
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Disorder Of Connective Tissue
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Connective Tissue Disorders
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|
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| Leukemia, Acute Lymphoblastic |
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Acute Lymphoblastic Leukemia
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ALL
|
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Acute Lymphocytic Leukemia
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Leukemia, Acute Lymphocytic, Susceptibility To, 1
|
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Acute Lymphoblastic Leukaemia
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Precursor Lymphoblastic Lymphoma/Leukemia
|
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Precursor Lymphoid Neoplasm
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Leukemia, Acute Lymphoblastic, Susceptibility To
|
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B-Cell Acute Lymphoblastic Leukemia
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Leukemia, Acute Lymphocytic 1
|
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Acute Lymphocytic Leukaemia
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Acute Lymphoblastic Leukemia/Lymphoma
|
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All1
|
Childhood Acute Lymphoblastic Leukemia
|
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Leukemia Acute Lymphoblastic 1
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Leukemia Acute Lymphoblastic B-Hyperdiploid
|
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Leukemia Acute Lymphocytic
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Leukemia Acute Lymphocytic 1
|
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Leukemia B-Cell Acute Lymphoblastic
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Leukemia T-Cell Acute Lymphoblastic
|
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Leukemia, Acute Lymphoblastic, 3
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ALL3
|
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Lymphoblastic Leukemia Acute
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Leukemia, Acute, Lymphoblastic
|
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Precursor Cell Lymphoblastic Leukemia Lymphoma
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Leukemia, Lymphocytic, Acute, L1
|
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Leukemia, Acute Lymphoblastic, Susceptibility To, 3
|
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| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
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Obesity, Susceptibility To
|
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Leanness, Inherited
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Obesity, Susceptibility To, Bmiq11
|
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Obesity, Mild, Early-Onset
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Obesity, Association With
|
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Obesity, Early-Onset, Susceptibility To
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Obesity, Severe
|
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Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
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Obesity , Susceptibility To
|
BMIQ11
|
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Obesity Bmiq11
|
Obesity, Early-Onset
|
|
Simple Obesity Nos
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Excess Fat
|
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Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
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| Retinitis Pigmentosa |
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RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
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Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
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Tapetoretinal Degeneration
|
Rcd
|
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Retinitis Pigmentosa Autosomal Recessive
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ARRP
|
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Retinitis Pigmentosa, Autosomal Recessive
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Retinitis Pigmentosa 1
|
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| Type 2 Diabetes Mellitus |
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Insulin Resistance
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NIDDM
|
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Type 2 Diabetes
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Diabetes Mellitus, Non-Insulin-Dependent
|
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T2D
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Noninsulin-Dependent Diabetes Mellitus
|
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Diabetes Mellitus, Type Ii
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Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
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Diabetes Mellitus, Type 2
|
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Diabetes Mellitus, Noninsulin-Dependent
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Diabetes Mellitus, Noninsulin-Dependent, Association With
|
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Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
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Non-Insulin-Dependent Diabetes Mellitus
|
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Type Ii Diabetes Mellitus
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Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
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Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
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Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
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Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
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Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
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Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
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|
