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Ontology Browser

Term:
Coffin-Siris Syndrome 7 (DOID:9009178)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
autosomal dominant non-syndromic intellectual disability 27  
Coffin-Siris syndrome 1  
Coffin-Siris Syndrome 10  
Coffin-Siris syndrome 2  
Coffin-Siris syndrome 3  
Coffin-Siris syndrome 4  
Coffin-Siris Syndrome 5  
Coffin-Siris syndrome 6  
Coffin-Siris Syndrome 7  
An autosomal dominant neurodevelopmental disorder characterized by global developmental delay with mild to moderate intellectual disability, speech impairment, behavioral abnormalities, poor overall growth, coarse facial features, and hypoplastic fifth toenails. (OMIM)
Coffin-Siris Syndrome 8  

Synonyms
Exact Synonyms: CSS7
Primary IDs: OMIM:618027

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