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
False vampire bat	Family Megadermatidae (organism)
familjär aktinisk prurigo	Actinic prurigo
Familial aplasia of the vermis	Familial aplasia of the vermis
Familial aplasia of the vermis	Familial aplasia of the vermis
benign familjär hyperkalcemi	Familial hypocalciuric hypercalcaemia
Familial cardiomyopathy	Familial cardiomyopathy
Familial cardiomyopathy	Familial cardiomyopathy
Familial chondrocalcinosis	Familial chondrocalcinosis
Familial dysautonomia	Familial dysautonomia
Familial dyskeratotic comedones	Familial dyskeratotic comedones
Familial gout with renal failure	Familial juvenile gout
Familial hyperkalemic periodic paralysis	Familial hyperkalemic periodic paralysis (disorder)
Familial hypophosphataemia	Familial x-linked hypophosphatemic vitamin D refractory rickets
Familial hypophosphataemic rickets	Familial x-linked hypophosphatemic vitamin D refractory rickets
Familial lipoprotein lipase deficiency	Familial hyperchylomicronemia
Familial lipoprotein lipase deficiency	Hyperlipoproteinemia, type I
familjär icke-polypös kolorektalcancer	HNPCC - hereditary nonpolyposis colon cancer
familjen Halarachnidae	Family Halarachnidae (organism)
familjen Trichocomacceae	Family Trichocomaceae (organism)
Family aware of diagnosis	Family aware of diagnosis
Family bovidae - bovid	Family Bovidae (organism)
Family callithricidae	Family Callitrichidae (organism)
Family caseworker	Family caseworker
Family circumstance NOS	Family circumstance NOS
Family circumstance NOS	Family circumstance NOS
Family circumstance NOS	Family circumstance NOS
Family circumstance NOS	Family circumstance NOS
Family counselled	Family counselled
Family counselling	Family counselling
Family culicidae - mosquito	Family Culicidae (organism)
Family desmodontidae	Subfamily Desmodontinae (organism)
Family disruption NOS	Family disruption NOS
Family disruption NOS	Family disruption NOS
familjeutbildning	Education of family
Family equidae - equid	Family Equidae (organism)
Family felidae - felid	Family Felidae (organism)
Family health history	Family history with explicit context (situation)
Family history	Family history with explicit context (situation)
Family history of alcoholism	Family history of alcoholism
Family history of breast cancer	Family history of malignant neoplasm of breast (situation)
Family history of learning difficulties	Family history of learning disability
Family history of mental disorder	Family history of mental disorder
Family history of pernicious anaemia	Family history of pernicious anemia
Family history of pernicious anaemia	Family history of pernicious anemia
hereditet för psykotiskt syndrom	Family history of psychotic illness (situation)
Family history of transient ischaemic attack	Family history of transient ischaemic attack
Family history of ulcerative colitis	FH: Ulcerative colitis
Family history taken	Family history taken
Family history: * - breast (context-dependent category)	Family history of neoplasm of breast
Family history: Addisonian anemia (context-dependent category)	Family history of pernicious anemia
Family history: Blood disorder NOS	FH: Blood disorder NOS
Family history: Brother NOS	FH: Brother NOS
Family history: COAD (context-dependent category)	Family history of chronic obstructive lung disease
Family history: CVA (context-dependent category)	Family history of stroke
hereditet för slaganfall eller stroke	Family history of stroke
Family history: CVS disease NOS	FH: CVS disease NOS
hereditet för hög kolesterolhalt	FH: Hypercholesterolemia
Family history: Congenital anomaly NOS	FH: Congenital anomaly NOS
Family history: Daughter NOS	FH: Daughter NOS
Family history: Ear disorder NOS	FH: Ear disorder NOS
Family history: Endocrine disorder NOS	FH: Endocrine disorder NOS
Family history: Eye disorder NOS	FH: Eye disorder NOS
Family history: Father NOS	FH: Father NOS
Family history: Gastrointestinal disorder NOS	FH: Gastrointestinal dis. NOS
Family history: Infectious disease NOS	FH: Infectious disease NOS
hereditet för hjärtinfarkt efter 60 års ålder	FH: Myocardial infarction at greater than 60
hereditet för hjärtinfarkt före 60 års ålder	FH: Myocardial infarction at less than 60
Family history: Mental disorder NOS	FH: Mental disorder NOS
Family history: Metabolic disorder NOS	FH: Metabolic disorder NOS
Family history: Mother NOS	FH: Mother NOS
familjeanamnes: sjuk mor	Maternal history of disorder
Family history: Musculo-skeletal disorder NOS	FH: Musculo-skeletal dis. NOS
Family history: NOS	FH: NOS
Family history: Relative NOS	FH: Relative NOS
Family history: Relative OS	FH: Relative OS
Family history: Respiratory disease NOS	FH: Respiratory disease NOS
Family history: Sister NOS	FH: Sister NOS
Family history: Skin disease NOS	FH: Skin disease NOS
Family history: Son NOS	FH: Son NOS
Family history: heart disease, congenital (context-dependent category)	FH: Congenital heart disease
Family history: neoplasm - NOS	FH: * - NOS
Family history: neoplasm - other intrathoracic organ	FH: * - other intrathorac org
Family history: neoplasm - other lymphoid/hematopoietic	FH: * - other lymph/haematop.
Family history: nervous system disorder (context-dependent category)	Family history of neurological disorder
Family hyaenidae - hyaenid	Family Hyaenidae (organism)
Family income supplement	Family income supplement (qualifier value)
Family lorisidae	Family Loridae (organism)
Family member on protection register	Family member on protection register
Family member removed from protection register	Family member removed from protection register (situation)
Family milestone NOS	Family milestone
Family milestone NOS	Family milestone
Family milestones	Family milestone
Family mustelidae - mustelid	Family Mustelidae (organism)
Family not aware of diagnosis	Family not aware of diagnosis
Family of man	Family Hominidae (organism)
utvärdering av analys av familjeprocesser	Assessment of family process
Family procyonidae - procyonid	Family Procyonidae (organism)
Family psychotherapy	Family psychotherapy procedure
Family pteropidae	Family Pteropodidae (organism)
Family record folder	Family record folder
Family viverridae - viverrid	Family Viverridae (organism)

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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)