Search Ontology:
Human Disease

Usher syndrome type 1B

Term ID
DOID:0070655
Synonyms
  • USH1B
  • Usher syndrome type IB
Definition
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the MYO7A gene on chromosome 11q13. https://pubmed.ncbi.nlm.nih.gov/7870171/
References
Ontology
Human Disease   ( DOID:0070655 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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