Disease #00052 (FANCA (FANCONI ANEMIA, COMPLEMENTATION GROUP A), OMIM:227650)

Official abbreviation FANCA
Name FANCONI ANEMIA, COMPLEMENTATION GROUP A
OMIM ID 227650
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FANCA
Associated tissues -
Disease features -
Remarks -
Date created 2020-03-03 15:58:40 +00:00 (UTC)
Date last edited 2023-06-16 09:10:23 +00:00 (UTC)

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