(Q5959167)

English

hypoalphalipoproteinemia

metabolic disorder characterized by deficiency of high density (alpha) lipoprotein in the blood

Hipoalfalipoproteinemia
Hypoalphalipoproteinemias

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Statements

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1 reference

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

APOA1

1 reference

stated in

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

NCI Thesaurus ID

C84774

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

http://purl.obolibrary.org/obo/HP_0003233

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003233

http://www.orpha.net/ORDO/Orphanet_31153

0 references

Identifiers

MeSH descriptor ID

D052456

mapping relation type

exact match

subject named as

Hypoalphalipoproteinemias

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

C16.320.565.398.500.330

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C18.452.584.500.875.330

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C18.452.648.398.500.330

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C18.452.584.563.500.330

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PatientsLikeMe condition ID

hypoalphalipoproteinemia

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1 reference

imported from Wikimedia project

English Wikipedia

GARD rare disease ID

2872

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Human Phenotype Ontology ID

HP:0003233

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003233

ICD-10

E78.6

1 reference

imported from Wikimedia project

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

5C81.0

Hypoalphalipoproteinaemia

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ICD-9 ID

272.5

1 reference

imported from Wikimedia project

English Wikipedia

Medical Dictionary for Regulatory Activities ID

10024626

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

Microsoft Academic ID

0 references

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1 reference

imported from Wikimedia project

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

1 reference

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003233

C0473527

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0003233

(Q5959167)

hypoalphalipoproteinemia

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