Cataract 41
Disease ID: disease_node_13692
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q12.0, MIM:116400 |
|---|---|
| Subclassof | DOID_0050736, DOID_83 |
| Data Source | DOID |
| Synonyms | CTRCT41, congenital nuclear type cataract 41 |
| Doid Label | cataract 41 |
| Doid Description | A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_13692 |
| Doid Id | DOID_0110241 |
| Label | Cataract 41 |
- Outgoing r'ship
SUBCLASS_OFto/from Cataract(ID:disease_node_1890;disease_node_13651) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)