Cataract 13 With Adult I Phenotype
Disease ID: disease_node_13691
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q12.0, MIM:116700 |
|---|---|
| Subclassof | DOID_83, DOID_0050737 |
| Data Source | DOID |
| Synonyms | CTRCT13 |
| Doid Label | cataract 13 with adult i phenotype |
| Doid Description | A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_13691 |
| Doid Id | DOID_0110242 |
| Label | Cataract 13 With Adult I Phenotype |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cataract(ID:disease_node_1890;disease_node_13651) (Disease)