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bn:00218030n
Noun Concept
Categories: Peroxisomal disorders
EN
D-bifunctional protein deficiency  17β-hydroxysteroid dehydrogenase 4 deficiency  17β-Hydroxysteroid dehydrogenase IV deficiency  17β-hydroxysteroid dehydrogenase type 4 deficiency  17β-Hydroxysteroid dehydrogenase type IV deficiency
EN
D-Bifunctional protein deficiency is an autosomal recessive peroxisomal fatty acid oxidation disorder. Wikipedia
Definitions
Relations
Sources
EN
D-Bifunctional protein deficiency is an autosomal recessive peroxisomal fatty acid oxidation disorder. Wikipedia
Human disease Wikidata
IS A
rare disease
genetic disease
peroxisomal disorder
GENETIC ASSOCIATION
HSD17B4
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
D-bifunctional protein deficiency
Wikidata
EN
D-bifunctional protein deficiency
Wikipedia Redirections
EN
17β-HSD 4 deficiency, 17β-HSD IV deficiency, 17β-HSD type 4 deficiency, 17β-HSD type IV deficiency, 17β-hydroxysteroid dehydrogenase 4 deficiency, 17β-Hydroxysteroid dehydrogenase 4 deficiency, 17β-Hydroxysteroid dehydrogenase IV deficiency, 17β-hydroxysteroid dehydrogenase IV deficiency, 17β-Hydroxysteroid dehydrogenase type 4 deficiency, 17β-hydroxysteroid dehydrogenase type 4 deficiency, 17β-Hydroxysteroid dehydrogenase type IV deficiency, 17β-hydroxysteroid dehydrogenase type IV deficiency, D-Bifunctional Protein Deficiency, HSD17B4 deficiency
Wikidata Alias
EN
17-Beta-Hydroxysteroid Dehydrogenase 4 Deficiency, 17-BETA-HYDROXYSTEROID DEHYDROGENASE IV DEFICIENCY, Bifunctional enzyme deficiency, D-Bifunctional Enzyme Deficiency, D-BIFUNCTIONAL PROTEIN DEFICIENCY, Dbp Deficiency, Multifunctional Enzyme Deficiency, Pbfe Deficiency, Peroxisomal Bifunctional Enzyme Deficiency, Peroxisomal Multifunctional Enzyme Deficiency, Pseudo-Zellweger Syndrome, Peroxisomal Multifunctional Enzyme (MFE2) Deficiency

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