complement component 6 deficiency

Preferred Label : complement component 6 deficiency;

MeSH note : mutation in C6 gene;

MeSH synonym : C6 deficiency;

Origin ID

C567307;

UMLS CUI

C2676232;

CISMeF manual mappings
- Complement component C6 deficiency [ICD-11 More detail]
Currated CISMeF NLP mapping
- Complement component 6 deficiency [OMIM Phenotype]
- complement component 6 deficiency [DO Concept]
MeSH term(s) associated for indexing
- Hereditary Complement Deficiency Diseases [MeSH Descriptor]
- complement C6 [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- complement component 6 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Complement component 6 deficiency [OMIM Phenotype]
- Complement component C6 deficiency [ICD-11 More detail]
- complement component 6 deficiency [DO Concept]