Search Ontology:
Human Disease

Usher syndrome type 3B

Term ID
DOID:0110842
Synonyms
  • USH3B
  • Usher syndrome type IIIB
Definition
An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31. https://www.ncbi.nlm.nih.gov/pubmed/22279524
References
Ontology
Human Disease   ( DOID:0110842 )
Relationships
is a type of
inverse disjoint_from
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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