268229003: Indeterminate sex and pseudohermaphroditism (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

400865010 Indeterminate sex and pseudohermaphroditism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

400866011 Gynandrism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

660944018 Indeterminate sex and pseudohermaphroditism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Indeterminate sex and pseudohermaphroditism	Is a	Congenital malformation of genital organs	false	Inferred relationship	Some
Indeterminate sex and pseudohermaphroditism	Occurrence	Congenital	false	Inferred relationship	Some
Indeterminate sex and pseudohermaphroditism	Finding site	Genital structure	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Course	Multiple superficial injuries of lower leg	false	Inferred relationship	Some
Indeterminate sex and pseudohermaphroditism	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Associated morphology	Congenital malformation	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Occurrence	Congenital	false	Inferred relationship	Some
Indeterminate sex and pseudohermaphroditism	Associated morphology	Congenital malformation	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Finding site	Genital structure	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Occurrence	Congenital	false	Inferred relationship	Some	2
Indeterminate sex and pseudohermaphroditism	Associated morphology	anomalie du développement	false	Inferred relationship	Some	2
Indeterminate sex and pseudohermaphroditism	Finding site	Genital structure	false	Inferred relationship	Some	2
Indeterminate sex and pseudohermaphroditism	Occurrence	Congenital	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
Indeterminate sex and pseudohermaphroditism	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Störung der Geschlechtsentwicklung 46,XX, ovotestikuläre	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
Pseudohermaphroditism	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
Pure gonadal dysgenesis	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
faux hermaphrodite	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
Indeterminate sex or pseudohermaphroditism NOS	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
Indeterminate sex NOS	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
Pseudohermaphrodite NOS	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations.	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some
46,XY ovotesticular disorder of sex development is a rare, genetic disorder of sex development characterized by either the coexistence of both male and female reproductive gonads or, more frequently, by the presence of one or both gonads containing a mixture of both testicular and ovarian tissue (ovotestes) in an individual with a normal male 46, XY karyotype. External genitalia are usually ambiguous but can range from normal male to normal female and if a uterus and/or fallopian tubes are present, they are generally hypoplastic. Cryptorchidism, hypospadias, infertility and increased risk of gonadal tumors are frequently associated.	Is a	False	Indeterminate sex and pseudohermaphroditism	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)