Cataract 17 Multiple Types
Disease ID: disease_node_13663
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q12.0, MIM:611544 |
|---|---|
| Subclassof | DOID_0050736, DOID_83, DOID_0050737 |
| Data Source | DOID |
| Synonyms | CTRCT17, CATCN3, autosomal recessive congenital nuclear cataract 3 |
| Doid Label | cataract 17 multiple types |
| Doid Description | A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12. |
| Has Material Basis In | GENO_0000147, GENO_0000148 |
| Disease Node Id | disease_node_13663 |
| Doid Id | DOID_0110270 |
| Label | Cataract 17 Multiple Types |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cataract(ID:disease_node_1890;disease_node_13651) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)