Hereditary Complement Deficiency Diseases
Disease ID: disease_node_529
Connections displayed (default: 10).
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| Dbxref | ICD10CM:D84.1, MESH:D000081208, NCI:C4691, SNOMEDCT_US_2023_03_01:191014008, UMLS_CUI:C0272242 |
|---|---|
| Subclassof | DOID_612 |
| Data Source | DOID, MESH |
| Synonyms | Complement deficiency disease |
| Mesh Id | D000081208 |
| Mesh Label | Hereditary Complement Deficiency Diseases |
| Mesh Subclassof | D000081207 |
| Doid Label | complement deficiency |
| Doid Description | A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predomitly in liver, which function to defend against infection and produce inflammation. |
| Has Phenotype | HP_0005339 |
| Disease Node Id | disease_node_529 |
| Doid Id | DOID_626 |
| Label | Hereditary Complement Deficiency Diseases |
- Incoming r'ship
SUBCLASS_OFto/from Type I Complement Component 8 Deficiency(ID:disease_node_20440) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Type Ii Complement Component 8 Deficiency(ID:disease_node_20439) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Immunologic Deficiency Syndromes(ID:disease_node_4256) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Complement Component 9 Deficiency(ID:disease_node_20438) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Complement Component 4B Deficiency(ID:disease_node_20441) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Complement Component 3 Deficiency(ID:disease_node_13253) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Complement Component 2 Deficiency(ID:disease_node_20442) (Disease) - Incoming r'ship
SUBCLASS_OFto/from C1 Inhibitor Deficiency(ID:disease_node_20437) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Atypical Hemolytic Uremic Syndrome(ID:disease_node_13080) (Disease)