Search Ontology:
Human Disease
autosomal recessive nonsyndromic deafness 119
- Term ID
- DOID:0070673
- Synonyms
-
- DFNB119
- Definition
- An autosomal recessive nonsyndromic deafness characterized by mild to profound sensorineural hearing loss that has_material_basis_in compound heterozygous mutation in the AFG2B gene on chromosome 15q21. https://pmc.ncbi.nlm.nih.gov/articles/PMC8546233/
- References
- Ontology
- Human Disease ( DOID:0070673 )
Other Pages
Genes Involved
Zebrafish Models