Disease #03542 (FANCG (Fanconi anemia, complementation group G (FANCG)), OMIM:614082)
Official abbreviation |
FANCG |
Name |
Fanconi anemia, complementation group G (FANCG) |
OMIM ID |
614082 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
153 |
Phenotype entries for this disease |
132 |
Associated with 1 gene |
FANCG |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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