Autosomal Recessive Nonsyndromic Deafness 67
Disease ID: disease_node_14997
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| Dbxref | ICD10CM:H90.3, MIM:610265 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB67, autosomal recessive deafness 67 |
| Doid Label | autosomal recessive nonsyndromic deafness 67 |
| 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 LHFPL5 gene on chromosome 6p21. |
| Disease Node Id | disease_node_14997 |
| Doid Id | DOID_0110518 |
| Label | Autosomal Recessive Nonsyndromic Deafness 67 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)