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Term:
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy (DOID:9008322)
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Parent Terms Term With Siblings Child Terms
alopecia +     
anodontia +     
Growth Disorders +     
3p- syndrome 
Acid-Labile Subunit Deficiency  
acrocapitofemoral dysplasia  
Acrocephalopolydactylous Dysplasia 
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 
ADULT syndrome  
Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations 
Al Gazali Khidr Prem Chandran Syndrome 
Al Kaissi Syndrome  
Aloi Tomasini Isaia Syndrome 
alopecia areata +   
Alopecia Congenita Keratosis Palmoplantaris +   
Alopecia Contractures Dwarfism Mental Retardation 
Alopecia Epilepsy Oligophrenia Syndrome of Moynahan 
alopecia universalis +   
Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia 
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia, Hypogonadism, Extrapyramidal Disorder 
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome  
Alopecia-Mental Retardation Syndrome +   
Androgenetic Alopecia 2 
Androgenetic Alopecia 3 
androgenic alopecia 
Anodontia of Permanent Dentition 
Aphalangia Syndactyly Microcephaly 
atrichia with papular lesions  
AUDITORY NEUROPATHY AND OPTIC ATROPHY  
Auriculoosteodysplasia 
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
Ayme-Gripp Syndrome  
Bainbridge-Ropers Syndrome  
Bellini Chiumello Rimoldi Syndrome 
Berk-Tabatznik Syndrome 
Bhaskar Jagannathan Syndrome 
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
Borjeson-Forssman-Lehmann syndrome  
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome  
Boudhina Yedes Khiari syndrome 
brachydactyly type E2  
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brooks-Wisniewski-Brown syndrome 
Bullous Dystrophy, Hereditary Macular Type 
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
Cantalamessa Baldini Ambrosi Syndrome 
Cantu Sanchez-Corona Fragoso Syndrome 
Cataract, Alopecia, Sclerodactyly 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Central Centrifugal Cicatricial Alopecia  
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy  
Charcot-Marie-Tooth disease X-linked recessive 5  
Chitty Hall Baraitser Syndrome 
chromosome 15q26-qter deletion syndrome 
chromosome 17q11.2 deletion syndrome, 1.4Mb  
Chromosome 18 Pericentric Inversion 
Clark-Baraitser Syndrome 
Cleft Palate, Deafness, and Oligodontia 
CODAS Syndrome  
Coffin Syndrome 1 
Congenital Alopecia X-Linked 
Cote Katsantoni Syndrome 
COUSIN SYNDROME  
Coxoauricular Syndrome 
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age 
Crumpled Helices and Small Mouth 
Curatolo Cilio Pessagno Syndrome 
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
Daish Hardman Lamont Syndrome 
Deafness Oligodontia Syndrome 
Dermatoosteolysis Kirghizian Type 
Dermatopathia Pigmentosa Reticularis  
Dermoids of Cornea 
Devriendt syndrome 
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Distal Renal Tubular Acidosis, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies 
DNA ligase IV deficiency  
Dubowitz syndrome 
Dyschondrosteosis and Nephritis 
Dysmyelinating Leukodystrophy with Oligodontia 
Ectodermal Dysplasia Alopecia Preaxial Polydactyly 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia, Trichoodontoonychial Type 
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation 
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
EVEN-PLUS SYNDROME  
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature  
Fallot Complex with Severe Mental and Growth Retardation 
Familial Focal Alopecia 
Familial Osteochondritis Dissecans  
Fetal Growth Retardation +   
Filippi Syndrome  
Floating-Harbor Syndrome  
Follicular Hamartoma, Alopecia, Cystic Fibrosis 
follicular mucinosis 
Forsythe-Wakeling Syndrome 
Frias Syndrome 
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 
Frontonasal Dysplasia 2  
Game Friedman Paradice Syndrome 
Garret Tripp Syndrome 
Gay Feinmesser Cohen Syndrome 
Geleophysic Dysplasia +   
GEMSS Syndrome  
Generalized Lipodystrophy, with Mental Retardation, Deafness, Short Stature, and Slender Bones 
Glomerulonephritis with Sparse Hair and Telangiectases  
GOMBO Syndrome 
Gomez Lopez Hernandez Syndrome 
Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Growth Deficiency and Mental Retardation with Facial Dysmorphism  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hagemoser Weinstein Bresnick Syndrome 
Hairy Elbows 
Heme Oxygenase 1 Deficiency  
hereditary spastic paraplegia 9A  
Hersh Podruch Weisskopk Syndrome 
Hooft Disease 
Hunter-McAlpine Syndrome 
Hutterite Cerebroosteonephrodysplasia Syndrome 
Hypergonadotropic Hypogonadism And Partial Alopecia 
Hypodontia Oligodontia with Orofacial Cleft 
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
hypoparathyroidism-retardation-dysmorphism syndrome  
hypotrichosis 7  
Ichthyosis Follicularis Atrichia Photophobia Syndrome  
Idiopathic Short Stature, X-Linked  
Insulin-Like Growth Factor I Deficiency  
Insulin-Like Growth Factor I, Resistance To  
Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein 
Jagell Holmgren Hofer Syndrome 
Johanson-Blizzard syndrome  
Johnson Neuroectodermal Syndrome 
Jorgenson Lenz Syndrome 
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant 
Konigsmark Knox Hussels Syndrome 
Kozlowski Rafinski Klicharska Syndrome 
Kuster Majewski Hammerstein Syndrome 
Ladda Zonana Ramer syndrome 
Langer Mesomelic Dysplasia  
Larsen Syndrome, Recessive Type  
Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy  
Leber hereditary optic neuropathy +   
Leri-Weill dyschondrosteosis  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Loose Anagen Hair Syndrome +   
Loucks-Innes Syndrome  
Lowry Maclean syndrome 
Lowry Wood Syndrome 
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis  
Macrosomia Adiposa Congenita 
Madelung Deformity 
Malocclusion and Short Stature 
mandibulofacial dysostosis with alopecia  
Megarbane Syndrome 
Mehta Lewis Patton Syndrome 
Meier-Gorlin syndrome +   
Mental and Growth Retardation with Amblyopia 
Mental Retardation Mietens Weber Type 
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature 
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism 
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy 
Microcephaly Cervical Spine Fusion Anomalies 
Microcephaly Sparse Hair Mental Retardation Seizures 
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2  
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1   
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2  
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES  
Microdontia Hypodontia Short Stature 
Milner Khallouf Gibson Syndrome 
Mitochondrial Myopathy with Lactic Acidosis  
Mollica Pavone Antener Syndrome 
Moloney Syndrome 
Morillo-Cucci Passarge Syndrome 
Multiform Ventricular Extrasystoles with Short Stature, Hyperpigmentation and Microcephaly 
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
Nathalie Syndrome 
Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult 
Neonatal Zinc Deficiency due to Low Breast Milk Zinc  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH  
Neurofaciodigitorenal Syndrome 
Nijmegen Breakage Syndrome-Like Disorder  
Nisch syndrome  
Ogden syndrome  
Oligodontia-Colorectal Cancer Syndrome  
Omodysplasia Type 1  
Onat Syndrome 
Optic Atrophy 1 and Deafness  
Optic Atrophy 10 with or without Ataxia, Mental Retardation, and Seizures  
Optic Atrophy 11  
Optic Atrophy 2 
Optic Atrophy 4 
Optic Atrophy 5  
Optic Atrophy 6 
Optic Atrophy 7  
Optic Atrophy 8  
Optic Atrophy 9  
Optic Atrophy and Cataract, Autosomal Dominant  
Optic Atrophy Spastic Paraplegia Syndrome 
Optic Atrophy with Demyelinating Disease of CNS 
Optic Atrophy with Negative Electroretinograms 
Optic Atrophy, Autosomal Dominant  
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Osteolysis Syndrome Recessive 
PARC Syndrome 
Partington Anderson Syndrome 
Patel Bixler Syndrome 
Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails 
Perniola Krajewska Carnevale Syndrome 
Peters plus syndrome  
Petty Laxova Wiedemann Syndrome 
Pfeiffer Kapferer Syndrome 
Pfeiffer Mayer Syndrome 
Pfeiffer Palm Teller Syndrome 
Pili Torti Developmental Delay Neurological Abnormalities 
Pilotto Syndrome 
Pinheiro Freire-Maia Miranda Syndrome 
Polydysspondyly 
Premature Aging, Okamoto Type 
Progeria Short Stature Pigmented Nevi 
Progeroid Syndrome, Congenital, Petty Type  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
PSPH deficiency  
Qazi Markouizos syndrome 
Radioulnar Synostosis Retinal Pigment Abnormalities 
Rajab Syndrome  
Ramon Syndrome 
Reardon Wilson Cavanagh Syndrome 
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome  
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa 
Rodrigues Blindness 
Rommen Mueller Sybert Syndrome 
Rowley-Rosenberg Syndrome 
Ruijs-Aalfs Syndrome  
Satoyoshi Syndrome 
Say Meyer Syndrome 
Say Syndrome 
Schaap Taylor Baraitser Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Scholte Syndrome 
Schopf-Schulz-Passarge Syndrome  
Seemanova Lesny Syndrome 
Senior-Loken syndrome +   
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation  
Severe Growth Restriction with Distinctive Facies  
Short Stature Syndrome, Brussels Type 
Short Stature, Amelogenesis Imperfecta, and Skeletal Dysplasia with Scoliosis  
Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly 
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
Short Stature, Optic Nerve Atrophy, and Pelger-Huet Anomaly  
SHORT Syndrome  
Single Upper Central Incisor  
Slavotinek Pike Mills Hurst Syndrome 
Slti Salem Syndrome 
Sonoda Syndrome 
Spastic Paraplegia, Optic Atrophy, and Dementia 
Spastic Paraplegia, Optic Atrophy, Microcephaly, and XY Sex Reversal 
Split-Hand and Split-Foot With Hypodontia 
Spondyloepimetaphyseal Dysplasia, Faden-Alkuraya Type  
spondyloepimetaphyseal dysplasia, Pakistani type  
Spondylometaphyseal Dysplasia, 'Corner Fracture' Type  
Stern Lubinsky Durrie Syndrome 
syndromic X-linked intellectual disability Cabezas type  
Synostosis of Talus and Calcaneus with Short Stature 
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
TATTON-BROWN-RAHMAN SYNDROME  
Taurodontia Absent Teeth Sparse Hair 
telogen effluvium 
Thai Symphalangism Syndrome 
THAUVIN-ROBINET-FAIVRE SYNDROME  
Theodor Hertz Goodman Syndrome 
Thrombocytopenia Robin Sequence 
Thumb Agenesis, Short Stature, and Immunodeficiency 
Thumb Deformity and Alopecia 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness 
Tonoki Syndrome 
tooth and nail syndrome  
Tsukahara Syndrome 
Turnpenny-Fry Syndrome  
Urban Schosser Spohn Syndrome 
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Verheij Syndrome  
Vertebral Body Fusion Overgrowth 
Viljoen Kallis Voges Syndrome 
Volcke Soekarman Syndrome 
Wellesley Carmen French Syndrome 
Wiedemann Grosse Dibbern Syndrome 
Winchester Syndrome  
Wittwer Syndrome 
Wolfram syndrome +   
Woodhouse Sakati Syndrome  
Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears 
X-Linked Hypodontia 
Young Hughes Syndrome 
Zadik Barak Levin Syndrome 
Zerres Rietschel Majewski Syndrome 

Synonyms
Exact Synonyms: GAPOS ;   Gapo syndrome ;   Odontotrichomelic Syndrome ;   tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
Primary IDs: MESH:C535642
Alternate IDs: OMIM:230740 ;   RDO:0000876

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.