Preferred Name

垂体功能减退症

Synonyms

卡尔门氏(KAllmAnn's)徵候群

性促素单独的缺乏

有生育力的宦官徵候群

席汉氏(SheehAn's)徵候群

脑垂腺身材矮小

脑垂腺恶病质

西蒙氏(SimmonDs')疾病

罗兰-莱威氏(LroAin-Levi)侏儒症

脑垂腺激素单独的缺乏

泛脑垂腺低能症

脑垂腺其他未明示的机能不全

脑垂腺坏死(产後)

生长素单独的缺乏

低性促素性腺低能症

自发性生长素缺乏症

ID

http://purl.bmicc.cn/ontology/ICD10CN/E23.0

altLabel

卡尔门氏(KAllmAnn's)徵候群

性促素单独的缺乏

有生育力的宦官徵候群

席汉氏(SheehAn's)徵候群

脑垂腺身材矮小

脑垂腺恶病质

西蒙氏(SimmonDs')疾病

罗兰-莱威氏(LroAin-Levi)侏儒症

脑垂腺激素单独的缺乏

泛脑垂腺低能症

脑垂腺其他未明示的机能不全

脑垂腺坏死(产後)

生长素单独的缺乏

低性促素性腺低能症

自发性生长素缺乏症

cui

C0020635

free_Translation

http://purl.bioontology.org/ontology/ICD10/E23.0

has_exact_match

http://purl.bioontology.org/ontology/ICD10/E23.0

hasDbXref

OMIM:308700

OMIM:614837

DOID:DOID_9410

OMIM:615271

OMIM:615266

OMIM:614858

DOID:DOID_0090093

DOID:DOID_0090072

OMIM:616030

OMIM:244200

DOID:DOID_0090076

OMIM:614841

OMIM:147950

OMIM:610628

OMIM:614839

OMIM:614838

OMIM:615267

DOID:DOID_0090084

DOID:DOID_0090073

ORDO:478

OMIM:614897

DOID:DOID_0090077

DOID:DOID_0090071

DOID:DOID_0090086

DOID:DOID_3614

OMIM:614842

OMIM:614840

DOID:DOID_0090080

DOID:DOID_0090079

DOID:DOID_0090082

OMIM:PS147950

OMIM:615269

ORDO:432

DOID:DOID_0090094

DOID:DOID_0090090

OMIM:612370

DOID:DOID_0090087

DOID:DOID_0090083

DOID:DOID_9476

DOID:DOID_0090092

OMIM:146110

DOID:DOID_0090070

DOID:DOID_0090085

DOID:DOID_0090074

OMIM:615270

DOID:DOID_0090078

DOID:DOID_9406

DOID:DOID_0090081

OMIM:612702

DOID:DOID_0090089

hasSTY

http://purl.bioontology.org/ontology/STY/T047

label

E23.0 垂体功能减退症

notation

E23.0

prefixIRI

ICD10CN:E23.0

prefLabel

垂体功能减退症

tui

T047

subClassOf

http://purl.bmicc.cn/ontology/ICD10CN/E23

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/E23.0 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU036880 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/MESH/D007018 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/OMIM/MTHU047352 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10/E23.0 International Classification of Diseases, Version 10 CUI