Autosomal Domit Nonsyndromic Deafness 41
Disease ID: disease_node_15089
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| Dbxref | ICD10CM:H90.3, MIM:608224 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA41, autosomal dominant deafness 41 |
| Doid Label | autosomal domit nonsyndromic deafness 41 |
| Doid Description | An autosomal domit nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in autosomal domit inheritance of heterozygous mutation in the purinergic receptor P2X 2 gene (P2RX2) on chromosome 12q24. |
| Disease Node Id | disease_node_15089 |
| Doid Id | DOID_0110567 |
| Label | Autosomal Domit Nonsyndromic Deafness 41 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)