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1234906009: 46,XX ovotesticular disorder of sex development (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5084684012 46,XX ovotesticular disorder of sex development (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084685013 46,XX ovotesticular disorder of sex development en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5400231010 A rare difference of sex development (DSD) characterized by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400232015 A rare difference of sex development (DSD) characterised by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5084684012 46,XX ovotesticular disorder of sex development (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084685013 46,XX ovotesticular disorder of sex development en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084686014 A rare disorder of sex development (DSD) characterized by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype. The cause is not elucidated for the majority of cases. A small proportion of individuals have a translocation of a Y chromosome fragment, including the SRY gene, to an X or another chromosome but most individuals (65%) are SRY negative. Some individuals may have a chromosomal mosaicism or a chimerism that results in the presence of Y chromosome containing cells in the gonad. The majority of cases arise as de novo gene variants. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5084687017 A rare disorder of sex development (DSD) characterised by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype. The cause is not elucidated for the majority of cases. A small proportion of individuals have a translocation of a Y chromosome fragment, including the SRY gene, to an X or another chromosome but most individuals (65%) are SRY negative. Some individuals may have a chromosomal mosaicism or a chimerism that results in the presence of Y chromosome containing cells in the gonad. The majority of cases arise as de novo gene variants. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400231010 A rare difference of sex development (DSD) characterized by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400232015 A rare difference of sex development (DSD) characterised by histologically confirmed testicular and ovarian tissue in an individual with a 46,XX karyotype. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3444601001000117 Störung der Geschlechtsentwicklung 46,XX, ovotestikuläre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3444601001000117 Störung der Geschlechtsentwicklung 46,XX, ovotestikuläre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
46,XX ovotesticular disorder of sex development (disorder) Is a 46,XX disorder of sex development true Inferred relationship Existential restriction modifier (core metadata concept)
46,XX ovotesticular disorder of sex development (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
46,XX ovotesticular disorder of sex development (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
46,XX ovotesticular disorder of sex development (disorder) Associated morphology Ovotestis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
46,XX ovotesticular disorder of sex development (disorder) Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
46,XX ovotesticular disorder of sex development (disorder) Is a Ovotesticular disorder of sex development true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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