abetalipoproteinemia (Q319812)
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Human disease
- familial hypobetalipoproteinemia
- microsomal triglyceride transfer protein deficiency disease
- Bassen-Kornzweig Syndrome
- Microsomal Triglyceride Transfer Protein Deficiency
- Bassen-Kornzweig disease
- Homozygous familial hypobetalipoproteinemia
- Mtp Deficiency
- ABETALIPOPROTEINEMIA
- ABL
- ABETALIPOPROTEINEMIA; ABL
- Acanthocytosis
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | abetalipoproteinemia |
Human disease |
|
Statements
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17 May 2019
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Abetalipoproteinemia
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Identifiers
Abetalipoproteinemia
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Sitelinks
Wikipedia(14 entries)
- arwiki فقد البروتين الشحمي بيتا من الدم
- dewiki Abetalipoproteinämie
- enwiki Abetalipoproteinemia
- eswiki Abetalipoproteinemia
- frwiki A-bêta-lipoprotéinémie
- hewiki אבטאליפופרוטאינמיה
- hrwiki Abetalipoproteinemija
- itwiki Abetalipoproteinemia
- plwiki Abetalipoproteinemia
- ptwiki Síndrome de Bassen-Kornzweig
- rowiki Abetalipoproteinemie
- srwiki Abetalipoproteinemija
- trwiki Abetalipoproteinemi
- ttwiki Бассен-Корнзвейг синдромы
Wikibooks(0 entries)
Wikinews(0 entries)
Wikiquote(0 entries)
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Wikiversity(0 entries)
Wikivoyage(0 entries)
Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Abetalipoproteinemia