Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Aphasia

Synonyms

Mixed Aphasias

Definitions

A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia.

ID

http://purl.bioontology.org/ontology/MESH/D001037

altLabel

Mixed Aphasias

Aphasias, Post-Traumatic

Dysphasia, Global

Aphasia, Graphomotor

Aphasia, Acquired

Dysphasia

Anepias

Aphasia, Mixed

Functional Aphasia

Alogia

Intellectual Aphasia

Lichtheim Sign

Dysphasias, Global

Aphasias, Global

Semantic Aphasias

Dejerine-Lichtheim Phenomenon

Aphasia, Global

Aphasia, Functional

Post-Ictal Aphasia

Aphasia, Ageusic

Intellectual Aphasias

Alogias

Discriminatory Aphasia, Auditory

Aphasias, Post-Ictal

Progressive Aphasias

Aphasia, Semantic

Aphasias, Intellectual

Aphasias, Semantic

Aphasia, Intellectual

Aphasia, Post-Ictal

Aphasia, Post Traumatic

Aphasias, Mixed

Post-Ictal Aphasias

Aphasias, Functional

Aphasia, Auditory Discriminatory

Logamnesia

Mixed Aphasia

Global Aphasia

Logagnosias

Phenomenon, Dejerine-Lichtheim

Ageusic Aphasia

Graphomotor Aphasias

Commisural Aphasias

Syntactical Aphasias

Auditory Discriminatory Aphasias

Post-Traumatic Aphasia

Syntactical Aphasia

Auditory Discriminatory Aphasia

Lichtheims Sign

Aphasias, Syntactical

Aphasias, Ageusic

Dejerine Lichtheim Phenomenon

Progressive Aphasia

Aphasia, Post-Traumatic

Aphasias, Progressive

Aphasia, Syntactical

Global Dysphasias

Post-Traumatic Aphasias

Global Dysphasia

Sign, Lichtheim's

Aphasia, Commisural

Semantic Aphasia

Aphasias, Commisural

Logagnosia

Global Aphasias

Logasthenia

Discriminatory Aphasias, Auditory

Logamnesias

Aphasias, Auditory Discriminatory

Aphasia, Post Ictal

Ageusic Aphasias

Aphasia, Progressive

Lichtheim's Sign

Aphasias, Graphomotor

Acquired Aphasia

Logasthenias

Anepia

Graphomotor Aphasia

Functional Aphasias

Commisural Aphasia

AN

GEN or unspecified; prefer specifics

AQL

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

cui

C0750918

C0234482

C0973461

C0234474

C0454576

C0234462

C0003537

C0750919

C0234472

C0003546

C0750917

C0338457

C0750920

C0750921

C0234484

C0234476

C0234469

DC

1

definition

A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia.

DX

19630101

FX

D018887

HN

1963

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/Q000628

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

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

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/D018887

http://purl.bioontology.org/ontology/MESH/D004292

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D009155

http://purl.bioontology.org/ontology/MESH/D001184

http://purl.bioontology.org/ontology/MESH/D013342

http://purl.bioontology.org/ontology/MESH/D004454

Machine permutation

1963; for APHASIA, ACQUIRED see APHASIA, ACQUIRED 1991-1995, see APHASIA 1980-1990

Mapped from

http://purl.bioontology.org/ontology/MESH/C563997

MDA

19990101

MMR

19991103

MN

C10.597.606.150.500.800.100

C23.888.592.604.150.500.800.100

notation

D001037

prefLabel

Aphasia

TERMUI

T003166

T371940

T371937

T003167

T371931

T371936

T003165

T371941

T372429

T371930

T372430

T371935

T372434

T371942

T371934

T372432

T371939

T372443

T371933

T371943

T371938

T371932

T372433

T372431

TH

UNK (19XX)

NLM (1996)

NLM (2000)

NLM (1966)

tui

T048

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D013064

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http://purl.bioontology.org/ontology/OMIM/MTHU036651 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/MTHU036651 Online Mendelian Inheritance in Man LOOM
http://purl.bmicc.cn/ontology/ICD11CN/MA80.0 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/LNC/MTHU020799 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/LNC/MTHU020799 Logical Observation Identifier Names and Codes LOOM
http://purl.obolibrary.org/obo/SYMP_0000508 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036833 Online Mendelian Inheritance in Man CUI
http://purl.obolibrary.org/obo/DOID_0060046 Human Disease Ontology 123 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34393 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0003537 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0003537 MedlinePlus Health Topics LOOM
http://purl.bioontology.org/ontology/LNC/LA18262-8 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/LNC/LA18262-8 Logical Observation Identifier Names and Codes LOOM
http://purl.bioontology.org/ontology/ICD10CM/R47.01 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10CM/R47.01 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.bioontology.org/ontology/ICD10CM/R47.02 International Classification of Diseases, Version 10 - Clinical Modification CUI