Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

OBSOLETE: Langerhans cell histiocytosis in childhood and adulthood
Synonyms

OBSOLETE: Histiocytosis X in childhood and adulthood

OBSOLETE: Langerhans cell granulomatosis in childhood and adulthood

ID

http://www.orpha.net/ORDO/Orphanet_264955

alternative_term

OBSOLETE: Histiocytosis X in childhood and adulthood

OBSOLETE: Langerhans cell granulomatosis in childhood and adulthood

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=264955

label

OBSOLETE: Langerhans cell histiocytosis in childhood and adulthood

notation

ORPHA:264955

prefixIRI

ORDO:Orphanet_264955

prefLabel

OBSOLETE: Langerhans cell histiocytosis in childhood and adulthood

reason_for_obsolescence

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.Instead, consider using Langerhans cell histiocytosis

subClassOf

http://www.orpha.net/ORDO/Orphanet_C051

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http://purl.obolibrary.org/obo/MONDO_0017036 MONDO LOOM