Search Ontology:
Human Disease
autosomal recessive nonsyndromic deafness 98
- Term ID
- DOID:0110540
- Synonyms
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- autosomal recessive deafness 98
- DFNB98
- Definition
- An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TSPEAR gene on chromosome 21q22. https://www.ncbi.nlm.nih.gov/pubmed/22678063
- References
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- ICD10CM:H90.3
- MIM:614861
- Ontology
- Human Disease ( DOID:0110540 )
- is a type of
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