complement factor H deficiency

Preferred Label : complement factor H deficiency;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0563175;

UMLS CUI

C0398777;

Currated CISMeF NLP mapping
- Complement factor h deficiency [OMIM Phenotype]
- Immunodeficiency with factor H anomaly [ICD-11 More detail]
- Immunodeficiency with factor H anomaly [ORDO Disease]
Related record
- complement factor H deficiency [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Complement factor h deficiency [OMIM Phenotype]
- Factor H deficiency (disorder) [SNOMED CT concept]
- Immunodeficiency with factor H anomaly [ORDO Disease]
- Immunodeficiency with factor H anomaly [ICD-11 More detail]