Experimental Factor Ontology

Last uploaded: June 18, 2024

Preferred Name	obsolete_Omenn syndrome
Synonyms	Combined immunodeficiency with hypereosinophilia
Definitions	Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; see this term).
ID	http://www.orpha.net/ORDO/Orphanet_39041
Obsolete	true
database_cross_reference	OMIM:603554 MedDRA:10069097 ICD10:D81.8
definition	Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; see this term).
definition_citation	orphanet
deprecated	true
has_exact_synonym	Combined immunodeficiency with hypereosinophilia
label	obsolete_Omenn syndrome
obsoleted_in_version	3.41.0
prefLabel	obsolete_Omenn syndrome
reason_for_obsolescence	Replaced with Mondo term.
term replaced by	http://purl.obolibrary.org/obo/MONDO_0011338
subClassOf	http://www.w3.org/2002/07/owl#Thing

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Delete	Mapping To	Ontology	Source
	http://www.orpha.net/ORDO/Orphanet_39041	ORDO	SAME_URI