Disease #00118 (FANCO (FANCONI ANEMIA, COMPLEMENTATION GROUP O), OMIM:613390)
Official abbreviation |
FANCO |
Name |
FANCONI ANEMIA, COMPLEMENTATION GROUP O |
OMIM ID |
613390 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
RAD51C |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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