364644000: Functional observable (observable entity)

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

Descriptions:

Id Description Lang Type Status Case? Module

487809018 Functional observable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

770915015 Functional observable (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3769371000005118 træk vedr. funktion da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
træk vedr. funktion	Is a	Clinical history/examination observable (observable entity)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sexual relationship problem due to gender identity confusion (finding)	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Frotteurism	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Klismaphilia	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Sadomasochism	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Compulsive exhibitionism	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Sexual arousal by exposure of genitals to non-consenting prepubertal and postpubertal person (disorder)	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Sexual relationship problem due to sexual orientation confusion	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Alstrom syndrome	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Sexual relationship problem (finding)	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Epiphyseal dysplasia-hearing loss-dysmorphism syndrome is a rare multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Patients also present severe behavior disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns. There have been no further descriptions in the literature since 1992.	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Sexual orientation confusion (finding)	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Birth trauma deafness	Interprets	False	træk vedr. funktion	Inferred relationship	Some
Avlund mobility-tiredness scale	Is a	False	træk vedr. funktion	Inferred relationship	Some

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Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)