Search Ontology:
Human Disease

obsolete Usher syndrome type 1J

Term ID
DOID:0110836
Synonyms
  • USH1J
  • Usher syndrome type IJ
Definition
An Usher syndrome type 1 that has_material_basis_in caused by homozygous mutation in the CIB2 gene on chromosome 15q24. https://www.ncbi.nlm.nih.gov/pubmed/23023331
References
Obsolete
true
Secondary ID:
Merged into
autosomal recessive nonsyndromic deafness 48
Ontology
  ( DOID:0110836 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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