Search Ontology:
Human Disease
complement component 3 deficiency
- Term ID
- DOID:8354
- Synonyms
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- C3 deficiency
- Definition
- A complement deficiency that is characterized by deficiency of complement component 3 that increases susceptibility to infection and autoimmune diseases and has_material_basis_in autosomal recessive inheritance of mutation in the C3 gene on chromosome 19p13.3, has_symptom recurrent bacterial infections. https://www.omim.org/entry/613779
- References
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- MIM:613779
- NCI:C9468
- ORDO:280133
- SNOMEDCT_US_2023_03_01:771443008
- UMLS_CUI:C1332655
- Ontology
- Human Disease ( DOID:8354 )
- is a type of
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