Farber lipogranulomatosis (Q1396345)
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extremely rare autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase
- Acid Ceramidase Deficiency
- Farber Disease
- N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY
- FRBRL
Language | Label | Description | Also known as |
---|---|---|---|
English | Farber lipogranulomatosis |
extremely rare autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase |
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Statements
1 reference
C84710
1 reference
Identifiers
Farber Lipogranulomatosis
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(14 entries)
- arwiki مرض فاربر
- dewiki Farber-Syndrom
- enwiki Farber disease
- eswiki Enfermedad de Farber
- fawiki بیماری فاربر
- fiwiki Farberin tauti
- frwiki Maladie de Farber
- itwiki Malattia di Farber
- plwiki Choroba Farbera
- ptwiki Doença de Farber
- ruwiki Болезнь Фарбера
- srwiki Фарберова болест
- ukwiki Хвороба Фарбера
- zhwiki 法伯病