Disease #03498 (CGD-3 (granulomatous disease, chronic, autosomal recessive cytochrome b-positive, type 3), OMIM:613960)
Official abbreviation |
CGD-3 |
Name |
granulomatous disease, chronic, autosomal recessive cytochrome b-positive, type 3 |
OMIM ID |
613960 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
NCF4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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