monosomy type X
http://purl.obolibrary.org/obo/MONDO_0020466
SCTID:710008008
Orphanet:99226
MEDGEN:116607
icd11.foundation:95979116
NCIT:C36630
UMLS:C0242526
GARD:19676
http://identifiers.org/medgen/116607
http://identifiers.org/snomedct/710008008
http://purl.obolibrary.org/obo/Orphanet_99226
http://linkedlifedata.com/resource/umls/id/C0242526
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/95979116
MONDO:0020466
http://purl.obolibrary.org/obo/mondo/mondo-base#rare
http://purl.obolibrary.org/obo/mondo/mondo-base#otar
http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_subtype_of_a_disorder
http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare
http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare
http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_etiological_subtype
monosomy X
http://purl.obolibrary.org/obo/NCIT_C36630
http://purl.obolibrary.org/obo/MONDO_0019499
http://purl.obolibrary.org/obo/MONDO_0700027
http://purl.obolibrary.org/obo/MONDO_0020639