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46,XX disorder of sex development

^ http://purl.obolibrary.org/obo/MONDO_0017576

Conditions affecting individuals with 46,XX karyotype characterized by atypical development of one or more of the following: the gonads, the internal reproductive structures, the external reproductive/genital structures. [ NCIT:C127169 ]

Term info

database cross reference
  • MESH:D058489 (Orphanet:2982/e)
  • UMLS:C2936403 (Orphanet:2982/e)
  • NCIT:C127169 (MONDO:equivalentTo)
  • Orphanet:325697 (MONDO:mondoIsBroaderThanSource)
  • Orphanet:2982 (MONDO:equivalentTo)
  • SCTID:8800006 (MONDO:equivalentTo)
  • UMLS:CN776919 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

definition

Conditions affecting individuals with 46,XX karyotype characterized by atypical development of one or more of the following: the gonads, the internal reproductive structures, the external reproductive/genital structures.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_2982, http://identifiers.org/snomedct/8800006, http://purl.obolibrary.org/obo/NCIT_C127169, http://linkedlifedata.com/resource/umls/id/C2936403, http://linkedlifedata.com/resource/umls/id/CN776919, http://identifiers.org/mesh/D058489

has exact synonym

46,XX disorders of Sex development, 46,XX DSD, 46,XX differences of Sex development, female pseudohermaphroditism

id

MONDO:0017576

narrowMatch

http://purl.obolibrary.org/obo/Orphanet_325697

Term relations