205719003: 46, XX true hermaphrodite (disorder)

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

4713811000052114 46,XX äkta hermafrodit sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
46,XX äkta hermafrodit	Is a	Congenital chromosomal disease	false	Inferred relationship	Some
46,XX äkta hermafrodit	Is a	hermafroditism	false	Inferred relationship	Some
46,XX äkta hermafrodit	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Some
46,XX äkta hermafrodit	Occurrence	Congenital	false	Inferred relationship	Some
46,XX äkta hermafrodit	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
46,XX äkta hermafrodit	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some
46,XX äkta hermafrodit	Finding site	Gonadal endocrine structure	false	Inferred relationship	Some	2
46,XX äkta hermafrodit	Finding site	Chromosome structure	false	Inferred relationship	Some	1
46,XX äkta hermafrodit	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
46,XX äkta hermafrodit	Associated morphology	kongenital anomali	false	Inferred relationship	Some
46,XX äkta hermafrodit	Finding site	Chromosome structure	false	Inferred relationship	Some	1
46,XX äkta hermafrodit	Occurrence	Congenital	false	Inferred relationship	Some	1
46,XX äkta hermafrodit	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	1
46,XX äkta hermafrodit	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)