abetalipoproteinemia (Q319812): Difference between revisions
Jump to navigation
Jump to search
Kr.angelov (talk | contribs) Added reference to claim: WordNet 3.1 Synset ID (P8814): 14175366-n, #quickstatements; #temporary_batch_1654547478460 |
Removed claim: WikiProjectMed ID (P11143): Abetalipoproteinemia, дублирующееся значение / duplicate value Tag: Manual revert |
||||||||||||||
| (30 intermediate revisions by 12 users not shown) | |||||||||||||||
| description / uk | description / uk | ||||||||||||||
хвороба людини | |||||||||||||||
| description / hy | description / hy | ||||||||||||||
մարդու հիվանդություն | |||||||||||||||
| Property / subclass of: autosomal recessive metabolic cerebellar ataxia / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 3 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: autosomal recessive metabolic cerebellar ataxia / reference | |||||||||||||||
retrieved: 3 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: metabolic disease with dementia / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: metabolic disease with dementia / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: metabolic disease with intestinal involvement / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: metabolic disease with intestinal involvement / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: hypobetalipoproteinemia / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: hypobetalipoproteinemia / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: neurometabolic disease / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: neurometabolic disease / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: developmental anomaly of metabolic origin / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: developmental anomaly of metabolic origin / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: syndromic dyslipidemia / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: syndromic dyslipidemia / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: constitutional hemolytic anemia due to acanthocytosis / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: constitutional hemolytic anemia due to acanthocytosis / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: rare hereditary metabolic disease with peripheral neuropathy / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: rare hereditary metabolic disease with peripheral neuropathy / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: metabolic disease with pigmentary retinitis / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: metabolic disease with pigmentary retinitis / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of: intestinal disease due to fat malabsorption / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / subclass of: intestinal disease due to fat malabsorption / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / subclass of | |||||||||||||||
| Property / subclass of: disease of a particular individual / rank | |||||||||||||||
| Property / instance of: developmental defect during embryogenesis / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / instance of: developmental defect during embryogenesis / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / ICD-10-CM: E78.6 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 3 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / ICD-10-CM: E78.6 / reference | |||||||||||||||
retrieved: 3 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / Encyclopædia Britannica Online ID: topic/abetalipoproteinemia / qualifier | |||||||||||||||
subject named as: abetalipoproteinemia | |||||||||||||||
| Property / MeSH descriptor ID: D000012 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 Mondo ID: MONDO_0008692 retrieved: 3 July 2018
| |||||||||||||||
| Property / MeSH descriptor ID: D000012 / reference | |||||||||||||||
Mondo ID: MONDO:0008692 retrieved: 3 July 2018
| |||||||||||||||
| Property / Mondo ID | |||||||||||||||
| Property / Mondo ID: MONDO:0008692 / rank | |||||||||||||||
| Property / Mondo ID: MONDO:0008692 / reference | |||||||||||||||
retrieved: 3 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / Orphanet ID: 14 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 3 July 2018
Mondo ID: MONDO_0008692 | |||||||||||||||
| Property / Orphanet ID: 14 / reference | |||||||||||||||
retrieved: 3 July 2018
Mondo ID: MONDO:0008692 | |||||||||||||||
| Property / genetic association: MTTP / reference | |||||||||||||||
stated in: Open Targets Platform retrieved: 24 August 2023
reference URL: https://platform.opentargets.org/evidence/ENSG00000138823/MONDO_0008692 based on heuristic: inferred from an Open Targets association score over 0.7 | |||||||||||||||
| Property / subclass of | |||||||||||||||
| Property / subclass of: disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / instance of | |||||||||||||||
| Property / instance of: symptom or sign / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / MeSH tree code | |||||||||||||||
| Property / MeSH tree code: C18.452.584.563.500.440.500 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / PatientsLikeMe condition ID | |||||||||||||||
| Property / PatientsLikeMe condition ID: abetalipoproteinemia / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / UniProt disease ID | |||||||||||||||
| Property / UniProt disease ID: DI-00014 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / WikiProjectMed ID | |||||||||||||||
| Property / WikiProjectMed ID: Abetalipoproteinemia / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Mondo ID | |||||||||||||||
| Property / Mondo ID: MONDO_0008692 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 07:17, 15 June 2024
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
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
3 references
1 reference
Abetalipoproteinemia
0 references
Identifiers
Abetalipoproteinemia
1 reference
1 reference
1 reference
2 references
1 reference
2 references
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)
Wikisource(0 entries)
Wikiversity(0 entries)
Wikivoyage(0 entries)
Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Abetalipoproteinemia