complement component 4a deficiency

Preferred Label : complement component 4a deficiency;

MeSH note : mutation in C4A;

Origin ID

C565167;

UMLS CUI

C3280642;

Automatic exact mappings (from CISMeF team)
- Decreased serum complement C4a [HPO term]
Currated CISMeF NLP mapping
- Complement component 4a deficiency [OMIM Phenotype]
- complement component 4a deficiency [DO Concept]
MeSH term(s) associated for indexing
- Hereditary Complement Deficiency Diseases [MeSH Descriptor]
- complement C4a [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- complement component 4a deficiency [MeSH concept]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Complement component 4a deficiency [OMIM Phenotype]
- Decreased serum complement C4a [HPO term]
- complement component 4a deficiency [DO Concept]