| Diseases |
Alias |
|
| Tarsal-Carpal Coalition Syndrome |
|
TCC
|
Tarsal Carpal Coalition Syndrome
|
|
Nog-Related-Symphalangism Spectrum Disorder
|
|
|
| Brachydactyly, Type B2 |
|
Brachydactyly Type B2
|
BDB2
|
|
Brachydactyly B2
|
|
|
| Stapes Ankylosis With Broad Thumbs And Toes |
|
Stapes Ankylosis With Broad Thumb And Toes
|
Teunissen-Cremers Syndrome
|
|
Ankylosis Of Stapes, Hyperopia, Broad Thumbs, Broad First Toes, And Syndactyly
|
Stapes Ankylosis Syndrome Without Symphalangism
|
|
SABTS
|
|
|
| Multiple Synostoses Syndrome 1 |
|
Symphalangism-Brachydactyly Syndrome
|
SYNS1
|
|
Wl Syndrome
|
Deafness-Symphalangism Syndrome Of Herrmann
|
|
Facioaudiosymphalangism Syndrome
|
Synostoses Multiple With Brachydactyly
|
|
Synostoses, Multiple, With Brachydactyly
|
Symphalangism Brachydactyly Syndrome
|
|
Synostoses Syndrome, Multiple, 1
|
|
|
| Symphalangism, Proximal, 1a |
|
SYM1A
|
Sym1
|
|
Cushing Symphalangism
|
Hereditary Absence Of The Proximal Interphalangeal Joints
|
|
Proximal Symphalangism 1a
|
Symphalangism, Proximal 1a
|
|
Symphalangism, Proximal
|
|
|
| Multiple Synostoses Syndrome |
|
Symphalangism-Brachydactyly Syndrome
|
Deafness-Hermann Type Symphalangism Syndrome
|
|
Facio-Audio-Symphalangism
|
Hearing Loss-Hermann Type Symphalangism Syndrome
|
|
Wl Syndrome
|
Multiple Synostosis Syndrome
|
|
|
| Proximal Symphalangism |
|
Cushing'S Symphalangism
|
Symphalangism, Proximal
|
|
Hereditary Absence Of Proximal Interphalangeal Joints
|
Strasburger-Hawkins-Eldridge Syndrome
|
|
Strasburger-Hawkins-Eldridge-Hargrave-Mckusick Syndrome
|
Symphalangism, Proximal, 1a
|
|
Symphalangism, Proximal, 1b
|
Vessel'S Syndrome
|
|
Symphalangism, Cushing Type
|
|
|
| Ankylosis |
|
|
| Fibrodysplasia Ossificans Progressiva |
|
Myositis Ossificans Progressiva
|
Progressive Myositis Ossificans
|
|
FOP
|
Progressive Ossifying Myositis
|
|
Myositis Ossificans
|
Stone Man Syndrome
|
|
Man Of Stone
|
Myositis Ossificans Progressive
|
|
Diffuse Progressive Ossifying Polymyositis
|
Fibrodysplasia Ossificans Congenita
|
|
Myositis Ossificans Progressiva, Site Unspecified
|
Münchmeyer Disease
|
|
Fop - [Fibrodysplasia Ossificans Progressiva]
|
Progressive Myositis Ossificans Calcification
|
|
|
| Brachydactyly, Type B1 |
|
Brachydactyly Type B1
|
Brachydactyly Type B
|
|
BDB1
|
Brachydactyly, Type B
|
|
Bdb
|
Brachydactyly B1
|
|
|
| Synostosis |
|
|
| Synostoses, Tarsal, Carpal, And Digital |
|
Calcaneonavicular Coalition
|
Multiple Synostosis Syndrome
|
|
Synostoses, Tarsal, Carpal And Digital
|
|
|
| Otosclerosis |
|
|
| Brachydactyly |
|
|
| Radioulnar Synostosis |
|
Radio-Ulnar Synostosis Type 1
|
|
|
| Sclerosteosis |
|
Cortical Hyperostosis With Syndactyly
|
Sost
|
|
Cortical Hyperostosis-Syndactyly Syndrome
|
|
|
| Esophageal Atresia |
|
Tracheoesophageal Fistula
|
Congenital Atresia Of Esophagus
|
|
Congenital Imperforate Esophagus
|
Imperforate Esophagus
|
|
Oesophageal Atresia
|
Te Fistula
|
|
Tef
|
Tracheoesophageal Fistula With Or Without Esophageal Atresia
|
|
|
| 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
|
|
|
| Osseous Heteroplasia, Progressive |
|
Progressive Osseous Heteroplasia
|
POH
|
|
Osteoma Cutis
|
Familial Ectopic Ossification
|
|
Ectopic Ossification Familial Type
|
Ectopic Ossification
|
|
Heterotopic Ossification
|
Ectopic Ossification, Familial
|
|
Cutaneous Ossification
|
Myositis Ossificans Progressiva
|
|
Osteodermia
|
Osteosis Cutis
|
|
Ossification Heterotopic
|
Heteroplasia, Osseous, Progressive
|
|
Fibrodysplasia Ossificans Progressiva
|
|
|
| Farsightedness |
|
Hypermetropia
|
Hyperopia
|
|
Far-Sightedness
|
Farsighted
|
|
Long-Sighted
|
Long-Sightedness
|
|
|
| Humeroradial Synostosis |
|
Humero-Radial Fusion
|
Humero-Radial Synostosis
|
|
Ramer Ladda Syndrome
|
|
|
| Neural Tube Defects |
|
Spina Bifida
|
Neural Tube Defect
|
|
NTD
|
Neural Tube Defects, Susceptibility To
|
|
Spinal Dysraphism
|
Spina Bifida, Susceptibility To
|
|
Rachischisis
|
Cleft Spine
|
|
Open Spine
|
Hydrocele Spinalis
|
|
Neural Tube Defect Nos
|
Sb - [Spina Bifida]
|
|
Spinal Hernia Nos
|
Spinal Fissure Nos
|
|
|
| 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
|
|
|
| Brachydactyly, Type A2 |
|
Brachydactyly Type A2
|
BDA2
|
|
Mohr-Wriedt Type Brachydactyly
|
Brachymesophalangy Ii
|
|
Brachymesophalangy Type 2
|
Brachymesophalangy 2
|
|
Brachydactyly, Mohr-Wriedt Type
|
Brachydactyly A2
|
|
|
| Holoprosencephaly |
|
Holoprosencephaly Sequence
|
Hpe
|
|
Hpe - [Holoprosencephaly]
|
|
|
| Acromesomelic Dysplasia 2b |
|
Fibular Hypoplasia And Complex Brachydactyly
|
Du Pan Syndrome
|
|
AMD2B
|
Dupans
|
|
Acromesomelic Dysplasia-2b
|
Fibular Aplasia-Complex Brachydactyly Syndrome
|
|
|
| Sugarman Brachydactyly |
|
Brachydactyly With Major Proximal Phalangeal Shortening
|
Brachydactyly Of The Hands And Feet With Duplication Of The First Toes
|
|
Sugarman-Hager-Kulik Syndrome
|
Orofaciodigital Syndrome 3
|
|
|
| Brachydactyly, Type A1, C |
|
Brachydactyly Type A1c
|
BDA1C
|
|
Brachydactyly A1, C
|
Brachydactyly A1c
|
|
Brachydactyly Type A1 C
|
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Zygodactyly
|
|
Syndactyly, Type I
|
Sd1
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Symphalangism
|
|
Non-Syndromic Syndactyly
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| Bone Disease |
|
Bone Diseases
|
Skeletal Disease
|
|
Skeletal Disorder
|
Disorder Of Skeletal System
|
|
|
| Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 |
|
Eec Syndrome
|
Rudiger Syndrome 1
|
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1
|
EEC1
|
|
Eec Syndrome 1
|
Eec Syndrome-1
|
|
Walker-Clodius Syndrome
|
Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome
|
|
Eec
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome
|
|
Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
|
Ectrodactyly-Cleft Lip/Palate Syndrome
|
|
Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Cleft Palate
|
Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
|
|
Ectrodactyly, Ectodermal Dysplasia, Clefting Syndrome
|
Ectrodactyly-Cleft Lip-Palate Syndrome
|
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome
|
|
|
| Juvenile Polyposis Syndrome |
|
JPS
|
Juvenile Intestinal Polyposis
|
|
Jip
|
Pji
|
|
Juvenile Gastrointestinal Polyposis
|
Juvenile Polyposis
|
|
Polyposis, Juvenile Intestinal
|
Polyposis, Familial, Of Entire Gastrointestinal Tract
|
|
Polyposis Familial Of Entire Gastrointestinal Tract
|
Polyposis Juvenile Intestinal
|
|
Polyposis Syndrome, Juvenile
|
|
|
| Renal Fibrosis |
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Brachydactyly, Type A1 |
|
Brachydactyly Type A1
|
BDA1
|
|
Farabee-Type Brachydactyly
|
Farabee Type Brachydactyly
|
|
Brachydactyly Farabee Type
|
Brachydactyly, Farabee Type
|
|
Brachydactyly A1
|
Brachydactyly
|
|
|
| Brachydactyly, Type C |
|
Brachydactyly Type C
|
BDC
|
|
Brachydactyly Haws Type
|
Brachydactyly, Haws Type
|
|
Brachydactyly C
|
|
|
| Telogen Effluvium |
|
|
| Hereditary Mixed Polyposis Syndrome |
|
|
| Cleft Palate, Isolated |
|
Cleft Palate
|
Isolated Cleft Palate
|
|
CPI
|
Cp
|
|
Palatoschisis
|
Cleft Palate Isolated
|
|
Uranostaphyloschisis
|
Congenital Fissure Of Palate
|
|
Cleft Of Secondary Palate
|
|
|
| Dysostosis |
|
|
| Germ Cell And Embryonal Cancer |
|
Germ Cell And Embryonal Neoplasm
|
|
|
| Prostate Cancer |
|
Prostate Carcinoma
|
Prostate Cancer, Familial
|
|
Prostate Neoplasm
|
Prostate Cancer, Somatic
|
|
Prostate Cancer, Susceptibility To
|
Prostatic Cancer
|
|
Prostatic Neoplasms
|
Hereditary Prostate Cancer
|
|
Prostatic Neoplasm
|
Cancer Of Prostate
|
|
Carcinoma Of Prostate
|
Familial Prostate Cancer
|
|
Familial Prostate Carcinoma
|
Malignant Tumor Of Prostate
|
|
Malignant Neoplasm Of Prostate
|
Prostate Cancer, Familial, Susceptibility To
|
|
Malignant Tumor Of The Prostate
|
Ngp - New Growth Of Prostate
|
|
Tumor Of The Prostate
|
Prostate Cancer, Hereditary
|
|
Cancer Of The Prostate
|
Malignant Neoplasm Of The Prostate
|
|
Prostatic Carcinoma
|
PC
|
|
Prca
|
Cancer, Prostate
|
|
Malignant Prostatic Tumour
|
Malignant Tumour Of Prostate
|
|
Primary Prostate Cancer
|
Primary Malignant Neoplasm Of Prostate
|
|
Prostate Gland Cancer
|
|
|
| Bone Development Disease |
|
|
| Chromosomal Duplication Syndrome |
|
|
| Orofacial Cleft |
|
|
| Robinow Syndrome, Autosomal Recessive 1 |
|
Robinow Syndrome, Autosomal Recessive
|
Autosomal Recessive Robinow Syndrome
|
|
Covesdem Syndrome
|
RRS1
|
|
Costovertebral Segmentation Defect-Mesomelia Syndrome
|
Rrs
|
|
Costovertebral Segmentation Defect With Mesomelia, Formerly
|
Covesdem Syndrome, Formerly
|
|
Costovertebral Segmentation Defect With Mesomelia
|
Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals
|
|
Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly
|
Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals
|
|
Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly
|
Robinow, Autosomal Recessive Syndrome, Type 1
|
|
|
| Severe Combined Immunodeficiency |
|
Scid
|
Severe Combined Immunodeficiency Disease
|
|
Combined T And B Cell Inborn Immunodeficiency
|
Immunodeficiency, Severe Combined
|
|
Scid - [Severe Combined Immunodeficiencies]
|
|
|
| Colonic Benign Neoplasm |
|
Colon Neoplasm
|
Colonic Mass
|
|
Colonic Tumor
|
Neoplasm Of Colon
|
|
Neoplasm Of The Colon
|
Colonic Neoplasms
|
|
Colon Cancer
|
Colon Carcinoma Nos
|
|
Colonic Cancer
|
Metastatic Colon Cancer Nos
|
|
|
| Hirschsprung Disease 1 |
|
Hirschsprung Disease
|
Aganglionic Megacolon
|
|
Hscr
|
Hirschsprung'S Disease
|
|
Congenital Megacolon
|
Congenital Intestinal Aganglionosis
|
|
Colonic Aganglionosis
|
Hirschsprung Disease, Susceptibility To, 1
|
|
Hirschsprung Disease, Protection Against
|
HSCR1
|
|
Mgc
|
Pelvirectal Achalasia
|
|
Total Intestinal Aganglionosis
|
Megacolon, Aganglionic
|
|
Macrocolon
|
Hscr 1
|
|
Hirschsprung Disease Type 1
|
Hirschsprung Disease, Type 1
|
|
Congenital Dilatation Of Colon
|
Aganglionosis
|
|
Congenital Aganglionic Megacolon
|
Aganglionosis Of Colon
|
|
Bowel Aganglionosis
|
Colon Aganglionosis
|
|
Hirschsprung Megacolon
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
