properdin deficiency, X-linked

Preferred Label : properdin deficiency, X-linked;

MeSH synonym : properdin P factor deficiency; properdin deficiency, type 1; properdin deficiency, type I;

Details

Origin ID

C537241;

UMLS CUI

C1839454;

Automatic exact mappings (from CISMeF team)
- X-linked properdin deficiency [DO Concept]
Currated CISMeF NLP mapping
- Immunodeficiency with properdin deficiency [ICD-11 More detail]
- Properdin deficiency [ORDO Disease]
- Properdin deficiency disease (disorder) [SNOMED CT concept]
- Properdin deficiency, X-linked [OMIM Phenotype]
- properdin deficiency disease [SNOMED Notion]
DO Cross reference
- X-linked properdin deficiency [DO Concept]
MeSH term(s) associated for indexing
- Hereditary Complement Deficiency Diseases [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- properdin [MeSH Descriptor]
ORDO relation(s)
- Properdin deficiency [ORDO Disease]
Record concept(s)
- Properdin deficiency, X-linked [MeSH concept]
See also inter- (CISMeF)
- properdin deficiency disease [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Properdin deficiency, X-linked [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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