chronic granulomatous disease
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency, mainly affecting phagocytes, which is characterized by an increased susceptibility to severe and recurrent bacterial and fungal infections, along with the development of granulomas. [ Orphanet:379 ]
Term info
- GARD:0006100 (MONDO:equivalentTo)
- Orphanet:379 (MONDO:equivalentTo)
- NCIT:C26788 (MONDO:equivalentTo)
- UMLS:C0018203 (Orphanet:379/e)
- OMIMPS:306400 (MONDO:equivalentTo)
- MESH:D006105 (Orphanet:379/e)
- MedDRA:10008906 (Orphanet:379/e)
- DOID:3265 (MONDO:equivalentTo)
- SCTID:387759001 (MONDO:equivalentTo)
gard_rare, ordo_disease
http://identifiers.org/meddra/10008906
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency, mainly affecting phagocytes, which is characterized by an increased susceptibility to severe and recurrent bacterial and fungal infections, along with the development of granulomas.
http://identifiers.org/snomedct/387759001, http://purl.obolibrary.org/obo/Orphanet_379, http://identifiers.org/mesh/D006105, https://omim.org/phenotypicSeries/PS306400, http://purl.obolibrary.org/obo/NCIT_C26788, http://purl.obolibrary.org/obo/DOID_3265, http://linkedlifedata.com/resource/umls/id/C0018203
http://purl.obolibrary.org/obo/MONDO_0015978, http://purl.obolibrary.org/obo/MONDO_0005265
CGD, chronic septic granulomatosis, congenital dysphagocytosis, Bridges-Good syndrome, Quie syndrome
granulomatous disease, chronic
MONDO:0018305
https://rarediseases.info.nih.gov/diseases/6100/chronic-granulomatous-disease