Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
Preferred Name

Androgen-Insensitivity Syndrome

Synonyms

Male Pseudohermaphroditism Due to Androgen Insensitivity

Definitions

A disorder also known as partial androgen insensitivity syndrome (PAIS). These patients exhibit partial resistance to androgenic and metabolic effects of TESTOSTERONE.

ID

http://purl.bioontology.org/ontology/MESH/D013734

altLabel

Male Pseudohermaphroditism Due to Androgen Insensitivity

Androgen Resistance Syndromes

Insensitivity Syndrome, Androgen

Testicular Feminizations

AR Deficiency

Reifensteins Syndrome

Androgen Insensitivity Syndrome, Partial

Insensitivity, Partial Androgen

Resistance Syndrome, Androgen

Androgen-Insensitivity Syndrome, Partial

Androgen-Insensitivity Syndromes

Androgen Insensitivity Syndromes

Deficiency, DHTR

Testicular Feminization Syndromes

Insensitivities, Partial Androgen

Receptor Deficiency, Androgen

Reifenstein Syndrome

Reifenstein's Syndrome

Partial Androgen Insensitivity

Resistance Syndromes, Androgen

Receptor Deficiencies, Dihydrotestosterone

Androgen-Insensitivity Syndromes, Partial

Deficiency, Dihydrotestosterone Receptor

Androgen Receptor Deficiency

Deficiency, AR

Insensitivity Syndromes, Androgen

Androgen Insensitivities, Partial

Dihydrotestosterone Receptor Deficiency

Androgen-Insensitivity Syndromes, Complete

Deficiencies, Dihydrotestosterone Receptor

Partial Androgen Insensitivities

Receptor Deficiency, Dihydrotestosterone

Deficiencies, Androgen Receptor

Testicular Feminization Syndrome

AR Deficiencies

Androgen Resistance Syndrome

Partial Androgen-Insensitivity Syndromes

Dihydrotestosterone Receptor Deficiencies

Deficiencies, DHTR

Feminization Syndromes, Testicular

Androgen Receptor Deficiencies

Partial Androgen-Insensitivity Syndrome

DHTR Deficiency

Androgen Insensitivity Syndrome, Complete

Deficiency, Androgen Receptor

Androgen-Insensitivity Syndrome, Complete

Feminization, Testicular

Feminization Syndrome, Testicular

Receptor Deficiencies, Androgen

Feminizations, Testicular

Androgen Insensitivity, Partial

Testicular Feminization

Deficiencies, AR

Complete Androgen-Insensitivity Syndromes

DHTR Deficiencies

Complete Androgen-Insensitivity Syndrome

Androgen Insensitivity Syndrome

AN

check the tag MALE

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

C0268301

C0039585

C0936016

C2713546

DC

1

definition

A disorder also known as partial androgen insensitivity syndrome (PAIS). These patients exhibit partial resistance to androgenic and metabolic effects of TESTOSTERONE.

A disorder of sexual development transmitted as an X-linked recessive trait. These patients have a karyotype of 46,XY with end-organ resistance to androgen due to mutations in the androgen receptor (RECEPTORS, ANDROGEN) gene. Severity of the defect in receptor quantity or quality correlates with their phenotypes. In these genetic males, the phenotypic spectrum ranges from those with normal female external genitalia, through those with genital ambiguity as in Reifenstein Syndrome, to that of a normal male with INFERTILITY.

A disorder also known as complete androgen insensitivity syndrome (CAIS). The 46,XY genetic male totally lacks androgen responsiveness in the target organs thus exhibits a female phenotype.

DX

19700101

HN

2002(1968)

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

2002; see TESTICULAR FEMINIZATION (1970-2001)

Mapped from

http://purl.bioontology.org/ontology/MESH/C538435

http://purl.bioontology.org/ontology/MESH/C564545

MDA

19990101

MMR

20210630

MN

C12.800.316.096.500

C12.200.706.316.096.500

C12.050.351.875.253.096.500

C19.391.119.096.500

C16.131.939.316.096.500

C16.320.322.061

notation

D013734

prefLabel

Androgen-Insensitivity Syndrome

TERMUI

T426481

T424068

T839576

T781892

T811924

T040334

T750927

T750926

T424067

T781893

T811923

T040333

T426480

T839575

T812205

TH

NLM (1998)

NLM (2002)

NLM (2010)

NLM (1968)

NLM (2012)

ORD (2010)

OMIM (2013)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D058490

http://purl.bioontology.org/ontology/MESH/D040181

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http://purl.bioontology.org/ontology/OMIM/300068 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/300068 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/DOID_4674 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_4674 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/312300 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/E34.5 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/ICD10CM/E34.5 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98812 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/OMIM/313700 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/313700 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/313700 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://www.orpha.net/ORDO/Orphanet_754 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27226 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/MONDO_0019154 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0019154 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/ICD10/E34.5 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10CM/E34.50 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/ICD10CM/E34.51 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/ICD10CM/E34.52 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bmicc.cn/ontology/ICD10CN/E34.5 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI