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Ontology Browser

Term:
Spondyloepimetaphyseal Dysplasia with Hypotrichosis (DOID:9001447)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
alopecia +   
anauxetic dysplasia 1  
Anauxetic Dysplasia 2  
autosomal recessive congenital ichthyosis 11  
autosomal recessive woolly hair 3  
Basaran Yilmaz Syndrome  
Bazex-Dupre-Christol Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
congenital hypotrichosis with juvenile macular dystrophy  
Dyggve-Melchior-Clausen disease +   
Ectodermal Dysplasia, Trichoodontoonychial Type 
hypohidrotic ectodermal dysplasia +   
hypotrichosis 1  
hypotrichosis 10 
hypotrichosis 11  
hypotrichosis 12  
hypotrichosis 13  
hypotrichosis 14  
hypotrichosis 2  
hypotrichosis 3  
hypotrichosis 4  
hypotrichosis 5 
hypotrichosis 6  
hypotrichosis 7  
hypotrichosis 8  
hypotrichosis 9 
hypotrichosis and recurrent skin vesicles  
hypotrichosis of eyelid 
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
hypotrichosis-lymphedema-telangiectasia syndrome +   
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Loucks-Innes Syndrome  
metatropic dysplasia  
Nicolaides Baraitser Syndrome  
Rombo syndrome 
Schimke immuno-osseous dysplasia  
Schopf-Schulz-Passarge syndrome  
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Spondyloepimetaphyseal Dysplasia with Hypotrichosis 
Spondyloepimetaphyseal Dysplasia with Joint Laxity +   
SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE  
Spondyloepimetaphyseal Dysplasia, Faden-Alkuraya Type  
spondyloepimetaphyseal dysplasia, Genevieve-type  
Spondyloepimetaphyseal Dysplasia, Irapa Type 
Spondyloepimetaphyseal Dysplasia, Isidor-Toutain Type  
Spondyloepimetaphyseal Dysplasia, Krakow Type  
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related  
spondyloepimetaphyseal dysplasia, Missouri type  
spondyloepimetaphyseal dysplasia, Pakistani type  
Spondyloepimetaphyseal Dysplasia, Shohat Type  
spondyloepimetaphyseal dysplasia, Sponastrime type  
spondyloepimetaphyseal dysplasia, Strudwick type  
Spondyloepimetaphyseal Dysplasia, X-Linked  
spondyloepiphyseal dysplasia congenita  
spondyloepiphyseal dysplasia tarda +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
Storm Syndrome 
Trichoodontoonychial Dysplasia 
X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy   

Synonyms
Exact Synonyms: Whyte Petersen McAlister syndrome ;   Whyte syndrome
Primary IDs: MESH:C535783
Alternate IDs: RDO:0001087

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