Disease #00205 (FANCU (FANCONI ANEMIA, COMPLEMENTATION GROUP U), OMIM:617247)

Official abbreviation FANCU
Name FANCONI ANEMIA, COMPLEMENTATION GROUP U
OMIM ID 617247
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene XRCC2
Associated tissues -
Disease features -
Remarks -
Date created 2024-06-03 15:32:06 +00:00 (UTC)
Date last edited N/A

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