familial c3b inhibitor deficiency syndrome

Preferred Label : familial c3b inhibitor deficiency syndrome;

Origin ID

DC-53070;

UMLS CUI

C0272243;

Currated CISMeF NLP mapping
- Familial C3B inhibitor deficiency syndrome (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Defects in the complement system [ICD-10 Sub-category (who)]
Metaterm(s)
- allergy and immunology [CISMeF Metaterm]
SNOMED CT concept
- Familial C3B inhibitor deficiency syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial C3B inhibitor deficiency syndrome (disorder) [SNOMED CT concept]