Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Myeloproliferative Disorders

Synonyms

Disorder, Myeloproliferative

Definitions

Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE.

ID

http://purl.bioontology.org/ontology/MESH/D009196

altLabel

Disorder, Myeloproliferative

Disorders, Myeloproliferative

Myeloproliferative Disorder

AN

myelo- here = bone marrow, not spinal cord; general; prefer specifics

AQL

BL CF CI CL CN 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

C0027022

DC

1

definition

Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE.

DX

19700101

FX

D007938

HN

70(66)

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/Q000151

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 RO

http://purl.bioontology.org/ontology/MESH/D007938

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D019046

http://purl.bioontology.org/ontology/MESH/D009190

http://purl.bioontology.org/ontology/MESH/D000741

http://purl.bioontology.org/ontology/MESH/D054437

Machine permutation

70

Mapped from

http://purl.bioontology.org/ontology/MESH/C565054

http://purl.bioontology.org/ontology/MESH/C564977

http://purl.bioontology.org/ontology/MESH/C566024

MDA

19990101

MMR

20070709

MN

C15.378.190.636

notation

D009196

prefLabel

Myeloproliferative Disorders

TERMUI

T027431

TH

NLM (1966)

tui

T191

subClassOf

http://purl.bioontology.org/ontology/MESH/D001855

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http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027022 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027022 MedlinePlus Health Topics LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU052356 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/MTHU010948 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/MTHU010939 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/D47.1 International Classification of Diseases, Version 10 - Clinical Modification CUI