Disorder of plasmalogens biosynthesis
MONDO:0017986Also known as: disorder of plasmalogens biosynthesis
3 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Rhizomelic chondrodysplasia punctata
(2)
Acyl-CoA binding domain containing protein 5 deficiency
(1)
Rhizomelic chondrodysplasia punctata type 1
(1)
Rhizomelic chondrodysplasia punctata type 2
(1)
Rhizomelic chondrodysplasia punctata type 3
(1)
Rhizomelic chondrodysplasia punctata type 5
(1)
Alkylglycerone-phosphate synthase deficiency
(0)
Fatty acyl-CoA reductase 1 deficiency
(0)
Fatty acyl-CoA reductase 1 upregulation
(0)
Fatty acyl-CoA reductase defects
(0)
Glyceronephosphate O-acyltransferase deficiency
(0)
Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain
(0)
Broader categories
Disease
(717)
Metabolic disease
(241)
Inherited lipid metabolism disorder
(199)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Human disease
(15)
Disease of genetic or genomic mechanism
(2)
Peroxisomal disease
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)