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

MVZ für Humangenetik Regensburg

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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