Autosomal Recessive Nonsyndromic Deafness 111
Disease ID: disease_node_14968
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| Dbxref | MIM:618145 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB111, autosomal recessive deafness 111 |
| Doid Label | autosomal recessive nonsyndromic deafness 111 |
| Doid Description | An autosomal recessive nonsyndromic deafness characterized by early-onset, moderate to severe sensorineural hearing loss with no vestibular involvement that has_material_basis_in homozygous or compound heterozygous mutation in the MPZL2 gene on chromosome 11q23.33. |
| Disease Node Id | disease_node_14968 |
| Doid Id | DOID_0111640 |
| Label | Autosomal Recessive Nonsyndromic Deafness 111 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)