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900000000000527005: SAME AS association reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Association type\Historical association reference set (foundation metadata concept)\SAME AS association reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

900000000001158011 SAME AS association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)
900000000001159015 SAME AS association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
SAME AS association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
FH: Brother	FH: Brother
FH: Brother NOS	Family history: Brother NOS
FH: Brother alive and well	FH: Brother alive and well
FH: Brother alive with problem	FH: Brother alive with problem
FH: Brother dead	Brother deceased (situation)
FH: CVA/stroke	Family history of stroke
FH: CVS disease NOS	Family history: CVS disease NOS
FH: Cardiomyopathy	FH: Cardiomyopathy
FH: Cardiomyopathy	FH: Cardiomyopathy
FH: Cataract	FH: Cataract
FH: Chromosomal anomaly	Family history of chromosomal anomaly (situation)
FH: Cong. orthopaedic anomaly	FH: Cong. orthopedic anomaly
FH: Congenital GIT anomaly	Family history: Congenital gastrointestinal tract anomaly (situation)
FH: Congenital GU anomaly	FH: Congenital GU anomaly
FH: Congenital RS anomaly	FH: Congenital RS anomaly
FH: Congenital anomaly	Family history of congenital disease (situation)
FH: Congenital anomaly NOS	Family history: Congenital anomaly NOS
FH: Congenital heart disease	FH: Congenital heart disease
FH: Consanguinity	Family history: Consanguinity (situation)
FH: Cystic fibrosis	Family history of cystic fibrosis (situation)
FH: Daughter	Family history with explicit context pertaining to daughter (situation)
FH: Daughter NOS	Family history: Daughter NOS
FH: Daughter alive and well	Family history: Daughter alive and well (situation)
FH: Daughter alive with problem	FH: Daughter alive with problem
FH: Daughter dead	Daughter deceased (situation)
FH: Deafness	FH: Deafness
FH: Death under 60 years	FH: Death under 60 years
FH: Depression	FH: Depression
FH: Diabetes mellitus	Family history of diabetes mellitus (situation)
FH: Dyslexia	FH: Dyslexia
FH: Dyslexia	FH: Dyslexia
FH: Ear disorder	Family history: Ear disorder (situation)
FH: Ear disorder NOS	Family history: Ear disorder NOS
FH: Early menarche	FH: Early menarche
FH: Early menopause	FH: Early menopause
FH: Eczema	FH: Eczema
FH: Endocrine disorder NOS	Family history: Endocrine disorder NOS
FH: Endocrine disorders	Family history of endocrine disorders (situation)
FH: Epilepsy	FH: Epilepsy
FH: Eye disorder	FH: Eye disorder
FH: Eye disorder NOS	Family history: Eye disorder NOS
FH: Father	Family history with explicit context pertaining to father (situation)
FH: Father NOS	Family history: Father NOS
FH: Father alive and well	Family history: Father alive and well (situation)
FH: Father alive with problem	FH: Father alive with problem
FH: Father dead	Father deceased
FH: Female infertility	FH: Female infertility
FH: Fragility fracture	FH: Fragility fracture
FH: Fragility fracture	FH: Fragility fracture
FH: Gastrointestinal dis. NOS	Family history: Gastrointestinal disorder NOS
FH: Gastrointestinal disease	FH: Gastrointestinal disease
FH: Glaucoma	FH: Glaucoma
FH: Gonorrhoea	FH: Gonorrhea
FH: Gout	FH: Gout
FH: Haemophilia	FH: Haemophilia
FH: Hay fever	FH: Hay fever
FH: Hay fever	FH: Hay fever
FH: Hemiplegia	FH: Hemiplegia
FH: Hip fracture in first degree relative	FH: Hip fracture in first degree relative
FH: Hip fracture in first degree relative	FH: Hip fracture in first degree relative
FH: Hirsutism	FH: Hirsutism
FH: Huntington's chorea	Family history: Huntington's chorea (situation)
FH: Hypercholesterolaemia	FH: Hypercholesterolemia
FH: Hypertension	FH: Hypertension
FH: Infantile cerebral palsy	Family history: Cerebral palsy
FH: Infectious disease	Family history of infectious disease (situation)
FH: Infectious disease NOS	Family history: Infectious disease NOS
FH: Ischaemic heart disease at greater than 60 years	FH: Ischemic heart disease at greater than 60 years
FH: Ischaemic heart disease at less than 60 years	FH: Ischaemic heart disease at less than 60 years
FH: Late menarche	FH: Late menarche
FH: Late menopause	FH: Late menopause
FH: Longevity	FH: Longevity
FH: Male infertility	FH: Male infertility
FH: Maternal grandfather	Family history with explicit context pertaining to maternal grandfather (situation)
FH: Maternal grandmother	Family history with explicit context pertaining to maternal grandmother (situation)
FH: Maternal hip fracture	FH: Maternal hip fracture
FH: Maternal hip fracture	FH: Maternal hip fracture
FH: Menstrual disorder	FH: Menstrual disorder
FH: Mental disorder NOS	Family history: Mental disorder NOS
FH: Metabolic disorder	Family history of metabolic disorder
FH: Metabolic disorder NOS	Family history: Metabolic disorder NOS
FH: Migraine	FH: Migraine
FH: Mother	Family history with explicit context pertaining to mother (situation)
FH: Mother NOS	Family history: Mother NOS
FH: Mother alive and well	Family history: Mother alive and well (situation)
FH: Mother alive with problem	FH: Mother alive with problem
FH: Mother dead	Mother deceased (situation)
FH: Motor neurone disease	Family history: Motor neurone disease (situation)
FH: Multiple sclerosis	FH: Multiple sclerosis
FH: Muscular dystrophy	FH: Muscular dystrophy
FH: Musculo-skeletal dis. NOS	Family history: Musculo-skeletal disorder NOS
FH: NOS	Family history: NOS
FH: Neoplasm of CNS	Family history of neoplasm of central nervous system (situation)
FH: Neoplasm of CNS	Family history of neoplasm of central nervous system (situation)
FH: Non-accidental injury to child	FH: Non-accidental injury to child
FH: Nutritional deficiency	FH: Nutritional deficiency
FH: Obesity	FH: Obesity
FH: Occupational lung dis.	Family history: Occupational lung disease (situation)
FH: Osteoarthritis	FH: Osteoarthritis
FH: Osteoporosis	Family history of osteoporosis
FH: Paraplegia	FH: Paraplegia

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001158011	SAME AS association reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001159015	SAME AS association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)