Autosomal Recessive Nonsyndromic Deafness 101
Disease ID: disease_node_15052
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| Dbxref | ICD10CM:H90.3, MIM:615837 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB101, autosomal recessive deafness 101 |
| Doid Label | autosomal recessive nonsyndromic deafness 101 |
| Doid Description | An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32. |
| Disease Node Id | disease_node_15052 |
| Doid Id | DOID_0110462 |
| Label | Autosomal Recessive Nonsyndromic Deafness 101 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)