Disease #00027 (FANCN (FANCONI ANEMIA, COMPLEMENTATION GROUP N), OMIM:610832)

Official abbreviation FANCN
Name FANCONI ANEMIA, COMPLEMENTATION GROUP N
OMIM ID 610832
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PALB2
Associated tissues -
Disease features -
Remarks -
Date created 2016-07-08 15:13:08 +00:00 (UTC)
Date last edited N/A

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