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Ontology Browser

Term:
Usher syndrome type 1D (DOID:0110831)
Annotations: Rat: (4) Mouse: (4) Human: (7) Chinchilla: (4) Bonobo: (4) Dog: (4) Squirrel: (4) Pig: (4)
Parent Terms Term With Siblings Child Terms
digenic disease +     
autosomal-mitochondrial sensorineural deafness  
facioscapulohumeral muscular dystrophy 2  
ocular albinism with sensorineural deafness  
retinitis pigmentosa 7  
Usher Syndrome Type 1B  
Usher syndrome type 1C  
Usher syndrome type 1D +   
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22. (DO)
Usher syndrome type 1E 
Usher syndrome type 1F +   
Usher syndrome type 1G  
Usher syndrome type 1H 
Usher syndrome type 1J  
Usher syndrome type 1K 
Usher Syndrome Type 1M  

Synonyms
Exact Synonyms: USH1D ;   USHER SYNDROME, TYPE ID
Primary IDs: MESH:C536487 ;   MESH:C563400
Alternate IDs: OMIM:601067 ;   RDO:0002089 ;   RDO:0012665
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/11138009 "DO"

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