Cataract 48
Disease ID: disease_node_13697
Connections displayed (default: 10).
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| Dbxref | MIM:618415 |
|---|---|
| Subclassof | DOID_0050737, DOID_83 |
| Data Source | DOID |
| Synonyms | CTRCT48 |
| Doid Label | cataract 48 |
| Doid Description | A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_13697 |
| Doid Id | DOID_0070354 |
| Label | Cataract 48 |
- 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)