Leber Congenital Amaurosis 7
Disease ID: disease_node_19106
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:613829 |
|---|---|
| Subclassof | DOID_0050177, DOID_14791 |
| Data Source | DOID |
| Synonyms | LCA7 |
| Doid Label | Leber congenital amaurosis 7 |
| Doid Description | A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13. |
| Disease Node Id | disease_node_19106 |
| Doid Id | DOID_0110333 |
| Disease Has Basis In | HP_0001197, SO_0000704 |
| Label | Leber Congenital Amaurosis 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Leber Congenital Amaurosis(ID:disease_node_12393) (Disease)