900000000000526001: REPLACED BY 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)\REPLACED BY 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

900000000001156010 REPLACED BY 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)

900000000001157018 REPLACED BY 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
REPLACED BY association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Family history: Mother NOS	Family history with explicit context pertaining to mother (situation)
Family history: Musculo-skeletal disorder NOS	FH: Musculoskeletal disease
Family history: NOS	Family history with explicit context (situation)
Family history: Relative NOS	Family history with explicit context (situation)
familieanamnese: slægtning, specificeret på anden måde	Family history with explicit context (situation)
Family history: Respiratory disease NOS	FH: Respiratory disease
familieanamnese: sklerodermi	Family history of scleroderma
Family history: Sister NOS	Family history with explicit context pertaining to sister (situation)
Family history: Skin disease NOS	FH: Skin disease
Family history: Son NOS	Family history with explicit context pertaining to son (situation)
Family history: neoplasm - NOS	Family history of neoplasm
Family history: neoplasm - other intrathoracic organ	Family history of neoplasm
Family history: neoplasm - other lymphoid/hematopoietic	Family history of neoplasm
Family hyposittidae	Family Vangidae (organism)
Family loriidae	Family Psittacidae (organism)
Family maladjustment	Family maladjustment
Family mimidae	Family Sturnidae (organism)
Family nycteribiidae - spiderlike bat fly	Subfamily Nycteribiinae (organism)
Family oxyruncidae	Family Cotingidae (organism)
Family pandionidae	Subfamily Pandioninae (organism)
Family phalaropodidae	Family Scolopacidae (organism)
Family phascolomidae - vombatidae	Family Vombatidae (organism)
Family poaceae - gramineae	Family Poaceae (organism)
Family pongidae	Family Hominidae (organism)
Family protelidae	Family Hyaenidae (organism)
Beroligelse af familie	Providing reassurance to family (situation)
Family recurvirostridae	Family Charadriidae (organism)
Family rhynchopidae	Family Laridae (organism)
Family tersinidae	Genus Tersina (organism)
Family tetraonidae	Subfamily Tetraoninae (organism)
Family vireolaniidae	Family Vireonidae (organism)
Family zeledoniidae	Genus Zeledonia (organism)
Farming/fishing manager NOS	Farming/fishing manager
Farming/fishing manager NOS	Farming/fishing manager
Fasciehernie på ben	Hernia of muscle through fascia of lower leg (disorder)
fascieløsningsteknik	Myofascial release (regime/therapy)
fasciotomi af anden specificeret lokalisation	Decompressive fasciotomy
Fast-electron therapy NOS	Fast-electron therapy
Fast-electron therapy NOS	Fast-electron therapy
fatal infektiøs mononukleose associeret med X-bundet lymfoproliferativt syndrom	A rare, genetic, primary immunodeficiency disorder characterised by an abnormal immune response to Epstein-Barr virus (EBV) infection, caused by hemizygous mutations in the X-linked SH2D1A gene, resulting in B cell lymphoproliferation and manifesting with various phenotypes which include EBV-driven severe or fulminant mononucleosis, haemophagocytic lymphohistiocytosis (presenting with fulminant hepatitis, hepatic necrosis, bone marrow hypoplasia, and neurological involvement), hypogammaglobulinaemia, and B-cell lymphoma. Additional variable manifestations include vasculitis, lymphomatoid granulomatosis, aplastic anaemia, and chronic gastritis. Occasionally, T-cell lymphoma may be observed. Laboratory findings include normal or increased activated T cells and reduced memory B cells.
patients far	Father
graviditetsbetinget træthed, barn født med postnatal komplikation	Fatigue during pregnancy
graviditetsbetinget træthed, ikke nærmere specificeret	Fatigue during pregnancy
graviditetsbetinget træthed, uspecificeret	Fatigue during pregnancy
graviditetsbetinget træthed med postnatal komplikation	Fatigue during pregnancy
faxrapport	Faxed report (record artifact)
Fækal og anden impaktation	Faecal impaction
Fecal occult blood NOS	Screening for occult blood in feces
Fecal occult blood: trace	Trace occult blood detected in feces
pankreatisk effekt på fæces	Feces pancreatic effects
Fecal sugars - general NOS	Detection of fecal reducing substances
Feces NOS	Examination of feces
Afføringsfarve, ikke nærmere specificeret	Color of stool
Afføringskonsistens, ikke nærmere specificeret	Examination of feces consistency
Feces examination - general NOS	Examination of feces
Feces examination NOS	Examination of feces
Afføringslugt, ikke nærmere specificeret	Odor of stool
Feces pH NOS	Measurement of feces pH
Afføringsmængde, ikke nærmere specificeret	Feces quantity
Feces sugar chromat. NOS	Faeces sugar chromatography
Afføringssymptomer, ikke nærmere specificeret	Faeces/motions - symptoms
fæces/afføring - symptomer	Finding of defecation
Feces: abnormal constituent NOS	Feces contents abnormal
Afføring: fremmedelement, ikke nærmere specificeret	Feces foreign constituent
Fechtners syndrom	MYH9-related disease (MYH9-RD) is an inherited giant platelet disorder with a complex phenotype characterized by congenital thrombocytopenia and possible subsequent manifestations of sensorineural hearing loss, presenile cataracts, elevation of liver enzymes, and/or progressive nephropathy often leading to end-stage renal disease (ESRD). Epstein syndrome, Fechtner syndrome, May-Hegglin anomaly and Sebastian syndrome, previously described as distinct disorders, represent some of the different clinical presentations of MYH9-RD.
Feeding intention - NOS	Feeding intention (finding)
Feeding intention - NOS	Feeding intention (finding)
Feeding problem NOS	Feeding problem
Feeding problem NOS	Feeding problem
Feline T-lymphotropic virus	Feline immunodeficiency virus
Felis pardina	Lynx pardinus (organism)
Felis planiceps	Prionailurus planiceps (organism)
Felis silvestris catus	Felis catus (organism)
Felis temmincki	Catopuma temminckii (organism)
Felis tigrinus	Leopardus tigrinus (organism)
Felis veverrinus	Prionailurus viverrinus (organism)
toksisk virkning af tuschpenne	Ink causing toxic effect
chlamydiainfektion i kvindelige bækken	Inflammation of pelvis caused by Chlamydia trachomatis (disorder)
kronisk pelvioperitonit hos kvinde	Chronic inflammation of pelvic peritoneum (disorder)
patients kvindelige forlovede	Female fiance
symptomer i relation til kvindeligt kønsorgan, ikke nærmere specificeret	Female genital organ symptoms
Female genital organ symptoms NOS	Female genital organ symptoms
Female genital symptoms NOS	Female genital organ symptoms
Kvindelige genitalsymptomer, ikke nærmere specificeret	Female genital organ symptoms
Female genital tract disorder NOS	Disorder of female genital system
sygdom tractus genitalis feminae, ikke nærmere specificeret	Disorder of female genital system
Female infertility NOS	Female infertility
Female infertility NOS	Female infertility
infertilitet hos kvinde, ikke nærmere specificeret	Female infertility
Female infertility associated with male factors	Failure to conceive due to infertility of male partner (finding)
Female infertility associated with male factors	Failure to conceive due to infertility of male partner (finding)
struktur af indre kvindelige kønsorganer	Structure of female genital system in pelvic cavity (body structure)
Female pelvic inflammatory disease NOS	Female pelvic inflammatory disease
inflammatorisk sygdom i kvindelige bækken, ikke nærmere specificeret	Female pelvic inflammatory disease
inflammatoriske sygdomme i kvindelige bækken, ikke nærmere specificeret	Female pelvic inflammatory disease
pelvin peritonit hos kvinde	Pelvic peritonitis
peritonit i kvindelige bækken, uspecificeret	Pelvic peritonitis
Female sex hormones NOS	Female sex hormones - serum measurement
Female sex hormones NOS	Female sex hormones - serum measurement
Female sterilisation reversal NOS	Reversal of female sterilization (procedure)
Female sterilization operation NOS	Female sterilization

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001156010	REPLACED BY 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)
900000000001157018	REPLACED BY association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)