Primary Congenital Glaucoma
Disease ID: disease_node_14333
Connections displayed (default: 10).
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| Dbxref | MIM:613085, MIM:613086 |
|---|---|
| Subclassof | DOID_0080015, DOID_1686, DOID_0050177 |
| Data Source | DOID |
| Doid Label | primary congenital glaucoma |
| Doid Description | A glaucoma that is characterized by damage to the optic nerves that reduces peripheral vision and leads to blindness, has_material_basis_in mutation in the MYOC gene and appears before the age of 5 without other associated abnormalities. Xref MGI. |
| Disease Node Id | disease_node_14333 |
| Doid Id | DOID_0050593 |
| Disease Has Basis In | HP_0001197, SO_0000704 |
| Label | Primary Congenital Glaucoma |
- Outgoing r'ship
SUBCLASS_OFto/from Glaucoma(ID:disease_node_3476) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hydrophthalmos(ID:disease_node_4066) (Disease)