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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
Eyelid inflammation	Blepharitis
Eyelid skin and periocular area laceration	Laceration of skin of eyelid AND periocular area
FEV1/FVC < 70% of predicted	FEV1/FVC < 70 percent of predicted
FEV1/FVC < 70% of predicted	FEV1/FVC < 70 percent of predicted
FEV1/FVC > 70% of predicted	Forced expiratory volume in one second/Forced vital capacity greater than 70 percent of predicted (finding)
FEV1/FVC > 70% of predicted	Forced expiratory volume in one second/Forced vital capacity greater than 70 percent of predicted (finding)
FEV1/FVC percent	FEV1/FVC percent
FEV1/FVC percent	FEV1/FVC percent
FEV1/FVC ratio abnormal	Forced expiratory volume in one second/forced vital capacity ratio abnormal (finding)
FEV1/FVC ratio normal	FEV1/FVC ratio normal
FH angina female first degree age known	FH angina female first degree age known
FH angina female first degree age known	FH angina female first degree age known
FH angina female first degree age unknown	FH angina female first degree age unknown
FH angina female first degree age unknown	FH angina female first degree age unknown
FH angina male first degree age known	FH angina male first degree age known
FH angina male first degree age known	FH angina male first degree age known
FH angina male first degree age unknown	FH angina male first degree age unknown
FH angina male first degree age unknown	FH angina male first degree age unknown
FH myocardial infarction female first degree age known	Family history of myocardial infarction in female relative of first degree, age known (situation)
FH myocardial infarction female first degree age known	Family history of myocardial infarction in female relative of first degree, age known (situation)
FH myocardial infarction female first degree age unknown	FH myocardial infarction female first degree age unknown
FH myocardial infarction female first degree age unknown	FH myocardial infarction female first degree age unknown
FH myocardial infarction male first degree age known	FH myocardial infarction male first degree age known
FH myocardial infarction male first degree age known	FH myocardial infarction male first degree age known
FH myocardial infarction male first degree age unknown	FH myocardial infarction male first degree age unknown
FH myocardial infarction male first degree age unknown	FH myocardial infarction male first degree age unknown
FH: * - breast	Family history of malignant neoplasm of breast (situation)
FH: * - leukaemia	Family history of leukemia
FH: * - male genital organ	Family history of neoplasm of male genital organ (situation)
FH: * - skin	Family history of neoplasm of skin (situation)
FH: Allergy	FH: Allergy
FH: Alzheimer's disease	FH: Alzheimer's disease
FH: Alzheimer's disease	FH: Alzheimer's disease
FH: Anaemia	FH: Anaemia
FH: Anencephaly	Family history: Anencephaly (situation)
FH: Ankylosing spondylitis	FH: Ankylosing spondylitis
FH: Ankylosing spondylitis	FH: Ankylosing spondylitis
FH: Aortic aneurysm	FH: Aortic aneurysm
FH: Aortic aneurysm	FH: Aortic aneurysm
FH: Asthma	Family history: Asthma (situation)
FH: Asthma	Family history: Asthma (situation)
FH: Atherosclerosis	FH: Atherosclerosis
FH: Atopy	FH: Atopy
FH: Aunt	Family history with explicit context pertaining to aunt (situation)
FH: Autoimmune disease	FH: Autoimmune disease
FH: Autoimmune disease	FH: Autoimmune disease
FH: Blood disorder	FH: Blood disorder
FH: Bowel cancer	FH: Bowel cancer
FH: Bowel cancer	FH: Bowel cancer
FH: Breast disease	FH: Breast disease
FH: Brother	FH: Brother
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: 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	FH: Congenital GIT anomaly
FH: Congenital GU anomaly	FH: Congenital GU anomaly
FH: Congenital RS anomaly	Family history of congenital respiratory system anomaly (situation)
FH: Congenital anomaly	Family history of congenital disease (situation)
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 alive and well	FH: Daughter alive and well
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	FH: Ear disorder
FH: Early menarche	FH: Early menarche
FH: Early menopause	Family history: Early menopause (situation)
FH: Eczema	FH: Eczema
FH: Endocrine disorders	Family history of endocrine disorders (situation)
FH: Epilepsy	FH: Epilepsy
FH: Eye disorder	FH: Eye disorder
FH: Father	Family history with explicit context pertaining to father (situation)
FH: Father alive and well	FH: Father alive and well
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 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	Family history of hip fracture in first degree relative (situation)
FH: Hip fracture in first degree relative	Family history of hip fracture in first degree relative (situation)

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Reference Sets

Reference set descriptor

GB English

US English

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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)