- ceramidase deficiency
- cer·am·i·dase de·fi·cien·cy (sə-ramґĭ-dās) Farber disease.
Medical dictionary. 2011.
ceramidase deficiency
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Ceramidase-Mangel — Klassifikation nach ICD 10 E75.2 Sonstige Sphingolipidosen (inkl. Farber Krankheit) … Deutsch Wikipedia
Ceramidase — is an enzyme which cleaves fatty acids from ceramide, producing sphingosine (SPH) which in turn is phosphorylated by a sphingosine kinase to form sphingosine 1 phosphate (S1P).[1] Contents 1 Function 2 Clinical significance … Wikipedia
ceramidase — An enzyme that hydrolyzes ceramides into sphingosine and a fatty acid; acylsphirgosine deacylase. A deficiency of this enzyme is associated with Farber disease. * * * cer·am·i·dase (sə ramґĭ dās) [EC 3.5.1.23] an enzyme of the… … Medical dictionary
Disseminierte Lipogranulomatose — Klassifikation nach ICD 10 E75.2 Sonstige Sphingolipidosen (inkl. Farber Krankheit) … Deutsch Wikipedia
Farber-Krankheit — Klassifikation nach ICD 10 E75.2 Sonstige Sphingolipidosen (inkl. Farber Krankheit) … Deutsch Wikipedia
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Morbus Farber — Klassifikation nach ICD 10 E75.2 Sonstige Sphingolipidosen (inkl. Farber Krankheit) … Deutsch Wikipedia
ASAH1 — N acylsphingosine amidohydrolase (acid ceramidase) 1, also known as ASAH1, is a human gene.cite web | title = Entrez Gene: ASAH1 N acylsphingosine amidohydrolase (acid ceramidase) 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
Farber disease — Classification and external resources ICD 10 E75.2 (ILDS E75.240) ICD 9 272.8 … Wikipedia
List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… … Wikipedia
