Usher Syndrome Type 1
Disease ID: disease_node_19175
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:276900, ORDO:231169 |
|---|---|
| Subclassof | DOID_0050439 |
| Data Source | DOID |
| Synonyms | US1, USH1 |
| Doid Label | Usher syndrome type 1 |
| Doid Description | An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa. |
| Disease Node Id | disease_node_19175 |
| Doid Id | DOID_0110826 |
| Label | Usher Syndrome Type 1 |
- Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1D(ID:disease_node_19182) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1J(ID:disease_node_19177) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1H(ID:disease_node_19178) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1G(ID:disease_node_19179) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1F(ID:disease_node_19181) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1C(ID:disease_node_19183) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1E(ID:disease_node_19180) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Usher Syndrome Type 1K(ID:disease_node_19176) (Disease)