Nephritis, Hereditary
Disease ID: disease_node_5489
Connections displayed (default: 10).
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| Dbxref | GARD:5785, MESH:D009394, ORDO:63, SNOMEDCT_US_2023_03_01:57333009, UMLS_CUI:C0027706 |
|---|---|
| Subclassof | DOID_225, DOID_0050177 |
| Data Source | DOID, MESH |
| Synonyms | Hereditary Nephritis |
| Mesh Id | D009394 |
| Mesh Label | Nephritis, Hereditary |
| Mesh Subclassof | D014564, D003095, D009393 |
| Doid Label | Alport syndrome |
| Doid Description | A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_5489 |
| Doid Id | DOID_10983 |
| Disease Has Basis In | SO_0000704 |
| Label | Nephritis, Hereditary |
- Incoming r'ship
SUBCLASS_OFto/from X-Linked Alport Syndrome(ID:disease_node_19098) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Autosomal Recessive Alport Syndrome(ID:disease_node_19099) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Autosomal Domit Alport Syndrome(ID:disease_node_19100) (Disease)