Fumaric aciduria Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Fumaric aciduria (FA), an autosomal recessive metabolic disorder, is most often characterized by early onset but non-specific clinical signs: hypotonia, severe psychomotor impairment, convulsions, respiratory distress, feeding difficulties and frequent cerebral malformations, along with a distinctive facies. Some patients present with only moderate intellectual impairment. (Orphanet Rare Disease Ontology, Orphanet_24)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538191
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Genes

1 genes/proteins associated with the disease Fumaric aciduria from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FH fumarate hydratase 2.88009