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Human Disease
autosomal recessive nonsyndromic deafness 88
- Term ID
- DOID:0110533
- Synonyms
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- autosomal recessive deafness 88
- DFNB88
- Definition
- An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ELMOD3 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/24039609
- References
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- ICD10CM:H90.3
- MIM:615429
- Ontology
- Human Disease ( DOID:0110533 )
- is a type of
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