granulomatous disease, chronic, autosomal recessive, cytochrome B-Positive, type II

Preferred Label : granulomatous disease, chronic, autosomal recessive, cytochrome B-Positive, type II;

MeSH note : mutation in NCF2;

MeSH synonym : granulomatous disease, chronic, due to NCF2 deficiency; P67-Phox, deficiency of; CGD, autosomal recessive cytochrome B-Positive, type II; neutrophil cytosol factor 2, deficiency of;

Details

Origin ID

C565531;

UMLS CUI

C1856245;

Automatic exact mappings (from CISMeF team)
- Granulomatous disease, chronic, autosomal recessive, 2 [OMIM Phenotype]
- autosomal recessive chronic granulomatous disease cytochrome b-positive type II [DO Concept]
MeSH term(s) associated for indexing
- NADPH Oxidases [MeSH Descriptor]
- granulomatous disease, chronic [MeSH Descriptor]
Record concept(s)
- granulomatous disease, chronic, autosomal recessive, cytochrome B-Positive, type II [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Granulomatous disease, chronic, autosomal recessive, 2 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients