Terminology Service for NFDI4Health

chronic granulomatous disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0018305


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. [ ]

Term info

Label

chronic granulomatous disease

Synonyms
  • Bridges-Good syndrome
  • CGD
  • Quie syndrome
  • chronic septic granulomatosis
  • congenital dysphagocytosis
database cross reference
Subsets

gard_rare, ordo_disease

closeMatch

http://identifiers.org/meddra/10008906

exactMatch

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

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015978, http://purl.obolibrary.org/obo/MONDO_0005265

has related synonym

granulomatous disease, chronic

id

MONDO:0018305

narrowMatch

https://icd.codes/icd10cm/D71

see also

https://rarediseases.info.nih.gov/diseases/6100/chronic-granulomatous-disease