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

5902551000172113 cariotype 46 XX de type hermaphrodisme fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4535631000172115 echt hermafroditisme met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4535641000172110 ovotestis met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4535651000172112 ovotesticulaire DSD met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4535661000172114 hermaphroditismus verus met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4535671000172117 ovotesticulaire geslachtsontwikkelingsstoornis met 46,XX-karyotype nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

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