Complement Component 2 Deficiency
Disease ID: disease_node_20442
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| Dbxref | GARD:1452, ICD10CM:D84.1, MIM:217000, ORDO:169147 |
|---|---|
| Subclassof | DOID_626 |
| Data Source | DOID |
| Doid Label | complement component 2 deficiency |
| Doid Description | A complement deficiency that is characterized by recurrent bacterial infections, has_material_basis_in autosomal recessive inheritance of mutation in the C2 gene. NT MGI. |
| Disease Node Id | disease_node_20442 |
| Doid Id | DOID_0060295 |
| Label | Complement Component 2 Deficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Hereditary Complement Deficiency Diseases(ID:disease_node_529) (Disease)