properdin deficiency, type II

Preferred Label : properdin deficiency, type II;

Origin ID

C564075;

UMLS CUI

C1839455;

Automatic exact mappings (from CISMeF team)
- Properdin deficiency, X-linked [OMIM Phenotype]
MeSH term(s) associated for indexing
- Hereditary Complement Deficiency Diseases [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
- properdin [MeSH Descriptor]
Record concept(s)
- properdin deficiency, type II [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]