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| Term | autosomal recessive nonsyndromic deafness 113 | ID (Ontology) | DOID:0111636 (Human Disease) |
| Definition | An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the CEACAM16 gene on chromosome 19q13. | ||
| Also Known As | "autosomal recessive deafness 113" ; "DFNB113" | ||
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nonsyndromic deafness________ autosomal recessive disease__| autosomal recessive nonsyndromic deafness |__autosomal recessive nonsyndromic deafness 113 |
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| Is a | autosomal recessive nonsyndromic deafness | ||
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| MIM:618410 | |||