Hirschsprung's disease
congenital disorder of digestive system
media legend: Гистопатология болезни Гиршпрунга
External resources
| Freebase ಐಡಿ | |
| MeSH descriptor ID | |
| Encyclopædia Britannica Online ID | science/congenital-megacolon subject named as: congenital megacolon |
| Quora topic ID | |
| YSO ID | |
| PatientsLikeMe condition ID | |
| DiseasesDB | |
| Orphanet ID | |
| Disease Ontology ID | |
| WikiProjectMed ID | |
| Genetics Home Reference Conditions ID | |
| MedlinePlus ID | |
| eMedicine ID | |
| MeSH tree code | |
| Human Phenotype Ontology ID | |
| Lex ID | |
| KEGG ID | |
| NL CR AUT ID | ph1062262 subject named as: Hirschsprungova nemoc |
| JSTOR topic ID (archived) | |
| NHS Health A to Z ID | |
| UMLS CUI | |
| ICD-11 ID (MMS) | LB16.1 subject named as: Hirschsprung disease |
| GARD rare disease ID | |
| OpenAlex ID | |
| ICD-11 ID (Foundation) | |
| OMIM ID | |
| ICD-10-CM | |
| Encyclopedia of China (Third Edition) ID | |
| J9U ID |
ಸ್ಮರಣಾರ್ಥ
Harald Hirschsprung
ಕಂಡುಹಿಡಿದ ಸಮಯ
1886[೧೧]
genetic association
external data available at URL
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
ಕಾಮನ್ಸ್ ವರ್ಗ
Hirschsprung's disease
Reference
- ↑ Freebase Data Dumps, ೨೮ ಅಕ್ಟೋಬರ್ 2013
- ↑ 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
- ↑ ೩.೦ ೩.೧ ೩.೨ ೩.೩ Human Phenotype Ontology release 2018-03-08, ೮ ಅಕ್ಟೋಬರ್ 2018, HP:0011286
- ↑ Quora
- ↑ YSO-Wikidata mapping project, ೩೧ ಜನವರಿ 2022
- ↑ ೬.೦ ೬.೧ ೬.೨ Disease Ontology, ೨೯ ನವೆಂಬರ್ 2020, DOID:10487
- ↑ UMLS 2023, ೨೫ ಮೇ 2023, inferred by common MeSH mappings on source and on Wikidata
- ↑ OpenAlex, ೨೬ ಜನವರಿ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ National Library of Israel Names and Subjects Authority File
- ↑ ೧೦.೦ ೧೦.೧ ೧೭ ಮೇ 2019, https://ddrare.nibiohn.go.jp/
- ↑ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637802/
- ↑ 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
- ↑ Identifiers.org, https://registry.identifiers.org/registry/doid