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Term:
autosomal dominant non-syndromic intellectual disability 27 (DOID:0070057)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (0) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
autosomal dominant mental retardation 20  
autosomal dominant mental retardation 45  
autosomal dominant mental retardation 46  
autosomal dominant mental retardation 47  
autosomal dominant mental retardation 48  
autosomal dominant mental retardation 49  
autosomal dominant mental retardation 50  
autosomal dominant mental retardation 51  
autosomal dominant mental retardation 52  
autosomal dominant mental retardation 53  
autosomal dominant mental retardation 54  
Autosomal Dominant Mental Retardation 57  
Autosomal Dominant Mental Retardation 58  
Autosomal Dominant Mental Retardation 60  
autosomal dominant non-syndromic intellectual disability 1  
autosomal dominant non-syndromic intellectual disability 10  
autosomal dominant non-syndromic intellectual disability 11  
autosomal dominant non-syndromic intellectual disability 13  
autosomal dominant non-syndromic intellectual disability 18  
autosomal dominant non-syndromic intellectual disability 19  
autosomal dominant non-syndromic intellectual disability 2  
autosomal dominant non-syndromic intellectual disability 21  
autosomal dominant non-syndromic intellectual disability 22  
autosomal dominant non-syndromic intellectual disability 23  
autosomal dominant non-syndromic intellectual disability 24  
autosomal dominant non-syndromic intellectual disability 26  
autosomal dominant non-syndromic intellectual disability 27  
An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of SOX11 on chromosome 2p25.2. (DO)
autosomal dominant non-syndromic intellectual disability 29  
autosomal dominant non-syndromic intellectual disability 3  
autosomal dominant non-syndromic intellectual disability 30  
autosomal dominant non-syndromic intellectual disability 31  
autosomal dominant non-syndromic intellectual disability 32  
autosomal dominant non-syndromic intellectual disability 33  
autosomal dominant non-syndromic intellectual disability 34  
autosomal dominant non-syndromic intellectual disability 35  
autosomal dominant non-syndromic intellectual disability 36  
autosomal dominant non-syndromic intellectual disability 38  
autosomal dominant non-syndromic intellectual disability 39  
autosomal dominant non-syndromic intellectual disability 4  
autosomal dominant non-syndromic intellectual disability 40  
autosomal dominant non-syndromic intellectual disability 41  
autosomal dominant non-syndromic intellectual disability 42  
autosomal dominant non-syndromic intellectual disability 43  
autosomal dominant non-syndromic intellectual disability 44  
autosomal dominant non-syndromic intellectual disability 5  
autosomal dominant non-syndromic intellectual disability 6  
autosomal dominant non-syndromic intellectual disability 7  
autosomal dominant non-syndromic intellectual disability 8  
autosomal dominant non-syndromic intellectual disability 9  
Coffin-Siris syndrome +   
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  
Coffin-Siris Syndrome 8  
Helsmoortel-Van Der Aa syndrome  
Koolen de Vries syndrome  
Schuurs-Hoeijmakers syndrome  
White-Sutton syndrome  
Xia-Gibbs syndrome  

Synonyms
Exact Synonyms: CSS9 ;   Coffin-Siris syndrome-9 ;   MRD27 ;   autosomal dominant mental retardation 27
Primary IDs: OMIM:615866
Alternate IDs: RDO:9001651
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/24886874

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