Autosomal Recessive Nonsyndromic Deafness 32
Disease ID: disease_node_15024
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| Dbxref | ICD10CM:H90.3, MIM:608653 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB32, HIIMS, autosomal recessive deafness 105, autosomal recessive deafness 32, hearing impairment infertile male syndrome |
| Doid Label | autosomal recessive nonsyndromic deafness 32 |
| Doid Description | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that has_material_basis_in mutation in the CDC14A gene on chromosome 1p21.2. |
| Disease Node Id | disease_node_15024 |
| Doid Id | DOID_0110491 |
| Label | Autosomal Recessive Nonsyndromic Deafness 32 |
| Doid Alternate Ids | DOID_0110466 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)