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fatty acyl-CoA reductase 1 deficiency

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive metabolic disorder clinically characterized by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity.
Mondo Term and Equivalent IDs
MONDO:0014510:  fatty acyl-CoA reductase 1 deficiency
Orphanet:438178: 
UMLS:C4015344: