Autosomal Recessive Nonsyndromic Deafness 36
Disease ID: disease_node_15021
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| Dbxref | ICD10CM:H90.3, MIM:609006 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB36, autosomal recessive deafness 36 |
| Doid Label | autosomal recessive nonsyndromic deafness 36 |
| Doid Description | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36. |
| Disease Node Id | disease_node_15021 |
| Doid Id | DOID_0110494 |
| Label | Autosomal Recessive Nonsyndromic Deafness 36 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)