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 -
Date created 2023-06-16 10:02:44 +00:00 (UTC)
Date last edited N/A

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