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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