complement component 3 deficiency, autosomal recessive

Preferred Label : complement component 3 deficiency, autosomal recessive;

MeSH synonym : C3 deficiency, autosomal recessive;

Origin ID

C565169;

UMLS CUI

C3151071;

Currated CISMeF NLP mapping
- C3D Format [NCIt concept]
- Complement component 3 deficiency [ORDO Disease]
- Complement component 3 deficiency, autosomal recessive [OMIM Phenotype]
- complement component 3 deficiency [DO Concept]
MeSH term(s) associated for indexing
- Hereditary Complement Deficiency Diseases [MeSH Descriptor]
- complement C3 [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- complement component 3 deficiency, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Complement component 3 deficiency [ORDO Disease]
- Complement component 3 deficiency, autosomal recessive [OMIM Phenotype]
Validated automatic mappings to NTBT
- C3 Deficiency [NCIt concept]
- Complement component 3 deficiency (disorder) [SNOMED CT concept]