Immunodeficiency syndrome, variable

Preferred Label : Immunodeficiency syndrome, variable;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531823;

UMLS CUI

C0398788;

Currated CISMeF NLP mapping
- Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder) [SNOMED CT concept]
- ICF syndrome [ORDO Disease]
- Immunodeficiency - centromeric region instability - facial anomalies syndrome [ICD-11 More detail]
- Immunodeficiency-centromeric instability-facial anomalies syndrome 1 [OMIM Phenotype]
- immunodeficiency, centromere instability and facial anomalies syndrome [Disease (Nov.)]
- immunodeficiency-centromeric instability-facial anomalies syndrome [DO Concept]
Related record
- immunodeficiency syndrome, variable [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder) [SNOMED CT concept]
- ICF syndrome [ORDO Disease]
- Immunodeficiency-centromeric instability-facial anomalies syndrome 1 [OMIM Phenotype]
- immunodeficiency, centromere instability and facial anomalies syndrome [Disease (Nov.)]
- immunodeficiency-centromeric instability-facial anomalies syndrome [DO Concept]