OBO ID: DOID:0112162
Term Name: autosomal recessive nonsyndromic deafness 116 Search Ontology:
Synonyms:
  • DFNB116
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous or compound heterozygous mutation in the CLDN9 gene on chromosome 16p13.3. https://pubmed.ncbi.nlm.nih.gov/31175426/
References:
Ontology: Human Disease   ( DOID:0112162 )
Relationships
is a type of:
OTHER autosomal recessive nonsyndromic deafness 116 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLDN9 ?Deafness, autosomal recessive 116
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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