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Human Disease

autosomal recessive nonsyndromic deafness 124

Term ID
DOID:0070676
Synonyms
  • DFNB124
Definition
An autosomal recessive nonsyndromic deafness characterized by congenital progressive sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the PKHD1L1 gene on chromosome 8q23. https://pmc.ncbi.nlm.nih.gov/articles/PMC11043200/
References
Ontology
Human Disease   ( DOID:0070676 )
Relationships
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Genes Involved
Zebrafish Models