complement component 7 deficiency

Preferred Label : complement component 7 deficiency;

MeSH note : mutation in C7 gene;

MeSH synonym : C7 deficiency;

Origin ID

C566443;

UMLS CUI

C1864694;

Currated CISMeF NLP mapping
- Complement component 7 deficiency [OMIM Phenotype]
- Complement component C7 deficiency [ICD-11 More detail]
- complement component 7 deficiency [DO Concept]
MeSH term(s) associated for indexing
- Hereditary Complement Deficiency Diseases [MeSH Descriptor]
- complement C7 [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- complement component 7 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Complement component 7 deficiency [OMIM Phenotype]
- Complement component C7 deficiency [ICD-11 More detail]
- complement component 7 deficiency [DO Concept]