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fumaric aciduria

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo 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.
Uniprot Description A severe autosomal recessive metabolic disorder characterized by early-onset hypotonia, profound psychomotor retardation, and brain abnormalities, such as agenesis of the corpus callosum, gyral defects, and ventriculomegaly. Many patients show neonatal distress, metabolic acidosis, and/or encephalopathy.
Mondo Term and Equivalent IDs
MONDO:0011730:  fumaric aciduria
DOID:0111261: 
GARD:0006476: 
MESH:C538191: 
Orphanet:24: 
SCTID:237983002: 
UMLS:C2936826: