205719003: echt hermafroditisme met 46,XX-karyotype (aandoening)

Status: retired, Not 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

315485011 46, XX true hermaphrodite en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591125012 46, XX true hermaphrodite (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

9209901000146110 ovotestis met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9458131000146119 echt hermafroditisme met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9458151000146113 hermaphroditismus verus met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9458161000146111 ovotesticulaire DSD met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9458171000146117 ovotesticulaire geslachtsontwikkelingsstoornis met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9493361000146114 echt hermafroditisme met 46,XX-karyotype (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
echt hermafroditisme met 46,XX-karyotype	Is a	Congenital chromosomal disease	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Is a	hermafroditisme (aandoening)	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Occurrence	Congenital	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Finding site	Gonadal endocrine structure	false	Inferred relationship	Some	2
echt hermafroditisme met 46,XX-karyotype	Finding site	Chromosome structure	false	Inferred relationship	Some	1
echt hermafroditisme met 46,XX-karyotype	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
echt hermafroditisme met 46,XX-karyotype	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some
echt hermafroditisme met 46,XX-karyotype	Finding site	Chromosome structure	false	Inferred relationship	Some	1
echt hermafroditisme met 46,XX-karyotype	Occurrence	Congenital	false	Inferred relationship	Some	1
echt hermafroditisme met 46,XX-karyotype	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	1
echt hermafroditisme met 46,XX-karyotype	Finding site	Chromosome structure	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

Description inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)