Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Hypoalphalipoproteinemias

Synonyms

HDL Lipoprotein Deficiency Disease

Definitions

Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS.

ID

http://purl.bioontology.org/ontology/MESH/D052456

altLabel

HDL Lipoprotein Deficiency Disease

Hypoalphalipoproteinemia, Familial

Lipoproteinemias, Hypo alpha

alpha Lipoproteinemia, Hypo

Lipoproteinemia, Hypo alpha

Hypo alpha Lipoproteinemia

HDL Cholesterol, Low Serum

Hypoalphalipoproteinemias, Familial

Familial High Density Lipoprotein Deficiency Disease

Hypoalphalipoproteinemias, Primary

alpha-Lipoprotein Deficiency Disease, Familial

alpha Lipoprotein Deficiency Disease, Familial

Hypoalphalipoproteinemia

Familial alpha Lipoprotein Deficiency Disease

Familial High-Density Lipoprotein Deficiency Disease

Hypo alpha Lipoproteinemias

High-Density Lipoprotein Deficiency Disease, Familial

Familial Hypoalphalipoproteinemias

Lipoprotein Deficiency Disease, HDL, Familial

Primary Hypoalphalipoproteinemias

Hypoalphalipoproteinemia, Primary

High Density Lipoprotein Deficiency Disease, Familial

Familial Hypoalphalipoproteinemia

Familial alpha-Lipoprotein Deficiency Disease

AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C1704429

C0473527

DC

1

definition

Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS.

DX

20070101

HN

2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL use TANGIER DISEASE 1995-2006

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D006995

Machine permutation

2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL see TANGIER DISEASE 1995-2006

Mapped from

http://purl.bioontology.org/ontology/MESH/C538394

MDA

20060705

MMR

20130708

MN

C18.452.648.398.500.330

C16.320.565.398.500.330

C18.452.584.500.875.330

notation

D052456

prefLabel

Hypoalphalipoproteinemias

TERMUI

T824988

T842563

T371755

T654660

T372519

T751034

T646278

T371758

T371756

T646277

T371743

T371742

T040051

TH

NLM (2000)

NLM (2010)

NLM (2007)

ORD (2010)

NLM (1995)

OMIM (2013)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D007009

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/E78.6 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU036760 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/604091 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/107680 Online Mendelian Inheritance in Man CUI