fanconi's anemia Gene Set

Dataset	DISEASES Curated Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A congenital hypoplastic anemia characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. It is a result of a genetic defect in a cluster of proteins responsible for DNA repair. (Human Disease Ontology, DOID_13636)
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Genes

18 genes involed in the disease fanconi's anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name
APITD1	apoptosis-inducing, TAF9-like domain 1
BRCA2	breast cancer 2, early onset
BRIP1	BRCA1 interacting protein C-terminal helicase 1
ERCC4	excision repair cross-complementation group 4
FANCA	Fanconi anemia, complementation group A
FANCB	Fanconi anemia, complementation group B
FANCC	Fanconi anemia, complementation group C
FANCD2	Fanconi anemia, complementation group D2
FANCE	Fanconi anemia, complementation group E
FANCF	Fanconi anemia, complementation group F
FANCG	Fanconi anemia, complementation group G
FANCI	Fanconi anemia, complementation group I
FANCL	Fanconi anemia, complementation group L
FANCM	Fanconi anemia, complementation group M
PALB2	partner and localizer of BRCA2
RAD51C	RAD51 paralog C
SLX4	SLX4 structure-specific endonuclease subunit
STRA13	stimulated by retinoic acid 13