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Ontology Browser

Term:
Spondyloepimetaphyseal Dysplasia with Hypotrichosis (DOID:9001447)
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Parent Terms Term With Siblings Child Terms
alopecia +   
Anauxetic Dysplasia +   
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 
Liberfarb Syndrome  
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, Borochowitz-Cormier-Daire Type  
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, Missouri type  
spondyloepimetaphyseal dysplasia, Pakistani type  
Spondyloepimetaphyseal Dysplasia, Shohat Type  
spondyloepimetaphyseal dysplasia, Sponastrime type  
spondyloepimetaphyseal dysplasia, Strudwick type  
spondyloepiphyseal dysplasia congenita  
spondyloepiphyseal dysplasia tarda +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
spondylometaepiphyseal dysplasia, short limb-hand type  
Storm Syndrome 
Trichoodontoonychial Dysplasia 
X-linked spondyloepimetaphyseal 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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