Autosomal Recessive Nonsyndromic Deafness 23
Disease ID: disease_node_15034
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| Dbxref | ICD10CM:H90.3, MIM:609533 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB23, autosomal recessive deafness 23 |
| Doid Label | autosomal recessive nonsyndromic deafness 23 |
| Doid Description | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the PCDH15 gene on chromosome 10q21. |
| Disease Node Id | disease_node_15034 |
| Doid Id | DOID_0110481 |
| Label | Autosomal Recessive Nonsyndromic Deafness 23 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)