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Hirschsprung's disease

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congenital disorder of digestive system

media legend: Гистопатология болезни Гиршпрунга

External resources

Freebase ಐಡಿ
/m/01t7bz[೧]
MeSH descriptor ID
D006627[೨][೩]

subject named as: Hirschsprung Disease

Encyclopædia Britannica Online ID
science/congenital-megacolon

subject named as: congenital megacolon

Quora topic ID
Hirschsprungs-Disease[೪]
YSO ID
22300[೫]

subject named as: Hirschsprungin tauti, Hirschsprungs sjukdom, Hirschsprung's disease

PatientsLikeMe condition ID
hirschsprung-s-disease
DiseasesDB
5901
Orphanet ID
388[೨]
Disease Ontology ID
DOID:10487[೬]
WikiProjectMed ID
Hirschsprung's disease
Genetics Home Reference Conditions ID
hirschsprung-disease
MedlinePlus ID
001140
eMedicine ID
178493
MeSH tree code
C06.198.439
C06.405.469.158.701.439
C16.131.314.439
Human Phenotype Ontology ID
HP:0011286[೩]
HP:0002251
Lex ID
Hirschsprungs_sygdom
KEGG ID
H00910
NL CR AUT ID
ph1062262

subject named as: Hirschsprungova nemoc

JSTOR topic ID (archived)
hirschsprung-disease
NHS Health A to Z ID
hirschsprungs-disease
UMLS CUI
C0019569[೨]
C0085758[೩]
C1257840[೭]
ICD-11 ID (MMS)
LB16.1

subject named as: Hirschsprung disease

GARD rare disease ID
6660[೨]
OpenAlex ID
C2779089422[೮]
ICD-11 ID (Foundation)
1772690306
OMIM ID
600156[೨]
606874[೨]
606875[೨]
608462[೨]
611644[೨]
ICD-10-CM
Q43.1[೨]
Encyclopedia of China (Third Edition) ID
630462
J9U ID
987007560557905171[೯]

ಉದಾಹರಣೆಗೆ

designated intractable/rare disease[೧೦]
class of disease

ಉಪವರ್ಗ

megacolon[೬]
intestinal dysganglionosis
ರೋಗ

ಸ್ಮರಣಾರ್ಥ

Harald Hirschsprung

ಕಂಡುಹಿಡಿದ ಸಮಯ

1886[೧೧]

health specialty

pediatrics
digestive system surgery
ಗ್ಯಾಸ್ಟ್ರೊಎಂಟೊರಾಲಾಜಿ

genetic association

NRG1[೧೨]

determination method or standard: genome-wide association study, TAS

external data available at URL

http://www.nanbyou.or.jp/entry/4699[೧೦]

language of work or name: ಜಪಾನಿ ಭಾಷೆ

described by source

Great Soviet Encyclopedia (1926–1947)

statement is subject of: Q98709125

on focus list of Wikimedia project

WikiProject Medicine

NCI Thesaurus ID

C34700[೨]

exact match

http://purl.obolibrary.org/obo/DOID_10487[೬]
http://identifiers.org/doid/DOID:10487[೧೩]
http://purl.obolibrary.org/obo/HP_0011286[೩]
http://www.orpha.net/ORDO/Orphanet_388

ಕಾಮನ್ಸ್ ವರ್ಗ

Hirschsprung's disease

Reference

  1. ↑ Freebase Data Dumps, ೨೮ ಅಕ್ಟೋಬರ್ 2013
  2. ↑ ೨.೦೦ ೨.೦೧ ೨.೦೨ ೨.೦೩ ೨.೦೪ ೨.೦೫ ೨.೦೬ ೨.೦೭ ೨.೦೮ ೨.೦೯ ೨.೧೦ Disease Ontology, ೧೫ ಮೇ 2019, DOID:10487
  3. ↑ ೩.೦ ೩.೧ ೩.೨ ೩.೩ Human Phenotype Ontology release 2018-03-08, ೮ ಅಕ್ಟೋಬರ್ 2018, HP:0011286
  4. ↑ Quora
  5. ↑ YSO-Wikidata mapping project, ೩೧ ಜನವರಿ 2022
  6. ↑ ೬.೦ ೬.೧ ೬.೨ Disease Ontology, ೨೯ ನವೆಂಬರ್ 2020, DOID:10487
  7. ↑ UMLS 2023, ೨೫ ಮೇ 2023, inferred by common MeSH mappings on source and on Wikidata
  8. ↑ OpenAlex, ೨೬ ಜನವರಿ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  9. ↑ National Library of Israel Names and Subjects Authority File
  10. ↑ ೧೦.೦ ೧೦.೧ ೧೭ ಮೇ 2019, https://ddrare.nibiohn.go.jp/
  11. ↑ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637802/
  12. ↑ Phenocarta, Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10487&ncbiId=3084, http://www.genome.gov/gwastudies/index.cfm?gene=NRG1, ೨೫ ಮೇ 2020
  13. ↑ Identifiers.org, https://registry.identifiers.org/registry/doid
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