Meesmann Corneal Dystrophy 2
Disease ID: disease_node_17142
Connections displayed (default: 10).
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| Dbxref | MIM:618767 |
|---|---|
| Subclassof | DOID_0050736, DOID_0060451 |
| Data Source | DOID |
| Doid Label | Meesmann corneal dystrophy 2 |
| Doid Description | A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17142 |
| Doid Id | DOID_0080671 |
| Label | Meesmann Corneal Dystrophy 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Corneal Dystrophy, Juvenile Epithelial Of Meesmann(ID:disease_node_11721) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)