Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
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Preferred Name

Anemia, Hemolytic, Congenital
Synonyms

Anemias, Congenital Hemolytic
Definitions

Hemolytic anemia due to various intrinsic defects of the erythrocyte.
ID

http://purl.bioontology.org/ontology/MESH/D000745
altLabel

Anemias, Congenital Hemolytic

Congenital Hemolytic Anemias

Hemolytic Anemia, Hereditary

Anemias, Hereditary Hemolytic

Hemolytic Anemias, Congenital

Anemia, Hereditary Hemolytic

Anemia, Hemolytic, Hereditary

Hereditary Hemolytic Anemia

Hemolytic Anemias, Hereditary

Anemia, Congenital Hemolytic

Congenital Hemolytic Anemia

Hereditary Hemolytic Anemias

Hemolytic Anemia, Congenital
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

C0002881
DC

1
definition

Hemolytic anemia due to various intrinsic defects of the erythrocyte.
DX

19680101
HN

68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64
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
Machine permutation

68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC was heading 1968-81, was ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1965-67
Mapped from

http://purl.bioontology.org/ontology/MESH/C566210

http://purl.bioontology.org/ontology/MESH/C536980

http://purl.bioontology.org/ontology/MESH/C535298

http://purl.bioontology.org/ontology/MESH/C566111

http://purl.bioontology.org/ontology/MESH/C536764

http://purl.bioontology.org/ontology/MESH/C563030

http://purl.bioontology.org/ontology/MESH/C566369

http://purl.bioontology.org/ontology/MESH/C564859

http://purl.bioontology.org/ontology/MESH/C566110

http://purl.bioontology.org/ontology/MESH/C563935

http://purl.bioontology.org/ontology/MESH/C562629
MDA

19990101
MMR

20090706
MN

C15.378.071.141.150

C16.320.070
notation

D000745
OL

use ANEMIA, HEMOLYTIC, CONGENITAL to search ANEMIA, CONGENITAL HEMOLYTIC 1966-67
prefLabel

Anemia, Hemolytic, Congenital
TERMUI

T002226

T002228

T002227

T002231

T002229

T002230
TH

NLM (1998)

NLM (1991)

NLM (1968)

ORD (2010)
tui

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D030342

http://purl.bioontology.org/ontology/MESH/D000743
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU052589 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/D58.9 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10/D58.9 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bmicc.cn/ontology/ICD10CN/D58.9 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI