Disease #06954 (CGD5 (chronic granulomatous disease, type 5), OMIM:618935)

Official abbreviation CGD5
Name chronic granulomatous disease, type 5
OMIM ID 618935
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene C17orf62
Associated tissues -
Disease features -
Remarks -
Date created 2022-08-12 17:27:32 +02:00 (CEST)
Date last edited N/A

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