OBO ID: DOID:0111738
Term Name: X-linked deafness 7 Search Ontology:
Synonyms:
  • DFNX7
  • X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
Definition: An X-linked nonsyndromic deafness characterized by congenital, bilateral, mixed or conductive hearing loss and other ear anomalies that has_material_basis_in homozygous or hemizygous mutation in the GPRASP2 gene on chromosome Xq22.1. https://www.ncbi.nlm.nih.gov/pubmed/28096187
References:
Ontology: Human Disease   ( DOID:0111738 )
Relationships
is a type of:
OTHER X-linked deafness 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GPRASP2 ?Deafness, X-linked 7
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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