Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 125

Term ID
DOID:0061124
Synonyms
  • autosomal recessive deafness 125
  • DFNB125
Definition
An autosomal recessive nonsyndromic deafness characterized by congenital nonsyndromic sensorineural hearing loss hat has_material_basis_in homozygous mutation in the GAS2 gene on chromosome 11p14. https://pubmed.ncbi.nlm.nih.gov/33964205/
References
Ontology
Human Disease   ( DOID:0061124 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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