Leber Congenital Amaurosis 9
Disease ID: disease_node_19110
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:608553 |
|---|---|
| Subclassof | DOID_0050737, DOID_14791 |
| Data Source | DOID |
| Synonyms | LCA9 |
| Doid Label | Leber congenital amaurosis 9 |
| Doid Description | A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19110 |
| Doid Id | DOID_0110005 |
| Disease Has Basis In | HP_0001197 |
| Label | Leber Congenital Amaurosis 9 |
- Outgoing r'ship
SUBCLASS_OFto/from Leber Congenital Amaurosis(ID:disease_node_12393) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)