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Human Disease
autosomal recessive nonsyndromic deafness 18B
- Term ID
- DOID:0110474
- Synonyms
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- autosomal recessive deafness 18B
- DFNB18B
- Definition
- An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/23122587
- References
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- ICD10CM:H90.3
- MIM:614945
- Ontology
- Human Disease ( DOID:0110474 )
- is a type of
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Zebrafish Models