Disease #00069 (FANCS (FANCONI ANEMIA, COMPLEMENTATION GROUP S), OMIM:617883)

Official abbreviation FANCS
Name FANCONI ANEMIA, COMPLEMENTATION GROUP S
OMIM ID 617883
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BRCA1
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 08:44:08 +00:00 (UTC)
Date last edited N/A

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