Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	Monosomy X
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_99226
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=99226
hasDbXref	ICD-10:Q96.9 ICD-11:LD50.00
label	Monosomy X
notation	ORPHA:99226 Etiological subtype
part_of	http://www.orpha.net/ORDO/Orphanet_881
prefixIRI	ORDO:Orphanet_99226
prefLabel	Monosomy X
treeView	http://www.orpha.net/ORDO/Orphanet_881
subClassOf	http://www.orpha.net/ORDO/Orphanet_557494

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_99226	CCONT	SAME_URI
http://www.orpha.net/ORDO/Orphanet_99226	EFO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0020466	MONDO	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/710008008	SNOMEDCT	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C36630	NCIT	LOOM
http://purl.obolibrary.org/obo/GSSO_007083	GSSO	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/737539006	SNOMEDCT	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_14199	HRDO	LOOM
http://purl.obolibrary.org/obo/NCIT_C36630	BERO	LOOM
http://purl.obolibrary.org/obo/MONDO_0020466	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0020466	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0020466	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0020466	KTAO	LOOM
http://www.gamuts.net/entity#Turner_syndrome	GAMUTS	REST