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Ontology Browser

Term:
Spondyloepimetaphyseal Dysplasia, Shohat Type (DOID:9006563)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
anauxetic dysplasia 1  
Anauxetic Dysplasia 2  
Dyggve-Melchior-Clausen disease +   
metatropic dysplasia  
Schimke immuno-osseous dysplasia  
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  
X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy   

Synonyms
Exact Synonyms: SEMD, Shohat Type ;   SEMDSH
Primary IDs: MESH:C566523
Alternate IDs: OMIM:602557 ;   RDO:0014855

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