900000000000531004: REFERS TO concept 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)\REFERS TO concept association reference set

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

900000000001166019 REFERS TO concept association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

900000000001167011 REFERS TO concept 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)

Expanded Value Set

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

Members	targetComponentId
Exophiala lecanii-corni	Exophiala lecanii-corni
Exophiala lecanii-corni (organism)	Exophiala lecanii-corni
Exostosis of elbow	Exostosis of elbow
Exostosis of femur	Exostosis of femur
Exostosis of foot	Exostosis of foot
Exostosis of scapula	Exostosis of scapula
Exostosis of tibia	Exostosis of tibia
Exploration of fascia of hand	Exploration of fascia of hand (procedure)
Exploration of inguinal canal	Exploration of inguinal canal
Exposure	Exposure to potentially harmful entity (event)
External	External
External condyle of humerus	Structure of lateral condyle of humerus (body structure)
External skeletal fixation	External fixation of bone
External skeletal fixation procedure	External fixation of bone
Extradural haemorrhage after injury	Traumatic intracranial extradural haemorrhage
Extradural hemorrhage after injury	Traumatic intracranial extradural haemorrhage
Extraocular muscle myectomy	Excision of extraocular muscle
Extravesical reimplantation of ureter	Extravesical reimplantation of left ureter (procedure)
Extravesical reimplantation of ureter	Extravesical reimplantation of right ureter
Extrinsic staining of teeth associated with drug	Extrinsic staining of teeth caused by drug
Exudative neurodermatitis	Exudative discoid eczema (disorder)
Eyelid inflammation	Inflammation of eyelid
FA - Fit complete fixed orthodontic appliance	Fitting of complete fixed orthodontic appliance
FA - Fluorescein angiography	Angiography of eye using fluorescein (procedure)
FB - Removal of foreign body from gingiva or periodontal ligament	Removal of foreign body from gingiva and supporting structure of tooth
FEP - Fibroepithelial polyp of oral mucosa	Fibroepithelial polyp of oral mucous membrane (disorder)
FHR - Fetal heart rate	Fetal heart rate
FNA - Fine needle aspiration of lesion of mastectomy scar	Fine needle aspiration biopsy of lesion of mastectomy scar
FT- Family therapy	Family therapy
Face to pubes delivery	Delivery of occipitoposterior presentation
Facet joint arthrogram	Facet joint arthrogram
Factor IX deficiency	Factor IX deficiency (disorder)
Factor XI deficiency	Factor XI deficiency
Faecal impaction of rectum	Fecal impaction of rectum (disorder)
Falloposcopy	Falloposcopy (procedure)
False hellebore	Veratrum
Familial Combined Hypercholesterolaemia	Familial combined hyperlipidemia
Familial Combined Hypercholesterolemia	Familial combined hyperlipidemia
Familial lecithin-cholesterol acyltransferase deficiency	A form of lecithin-cholesterol acyltransferase deficiency (LCAT) characterized clinically by corneal opacities, hemolytic anemia and renal failure and biochemically by severely decreased HDL cholesterol and complete deficiency of the LCAT enzyme. Age of onset and severity of clinical manifestations are variable. Caused by mutations in the LCAT gene (16q22.1) encoding the LCAT enzyme which catalyzes the formation of cholesterol esters in lipoproteins, leading to progressive lipid deposition in body tissues. There is no clear genotype-phenotype correlation since family members with the same mutation have been found to have different clinical and biochemical pictures. Environmental factors or other minor genes may therefore also be involved in the disorder.
Familial multiple fibrofolliculoma	A rare inherited cancer-predisposing syndrome characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. The kidney tumors range from benign oncocytomas to malignant renal cell carcinomas including chromophobe, clear cell or papillary subtypes. Fibrofolliculomas are characterized by a circumscribed proliferation of collagen and fibroblasts surrounding distorted hair follicles from which basaloid cells protrude into the surrounding fibromucinous stroma. Other characteristic skin anomalies are trichodiscomas and acrochordons. Dermatological manifestations usually develop in the third and fourth decades of life and persist indefinitely. The syndrome is transmitted in an autosomal dominant fashion.
Familial paroxysmal choreoathetosis	Paroxysmal nonkinesigenic dyskinesia (disorder)
Family history of cardiac arrhythmia	Family history of cardiac arrhythmia (situation)
Family history of familial hypercholesterolaemia	Family history of familial hypercholesterolemia (situation)
Family history of familial hypercholesterolemia	Family history of familial hypercholesterolemia (situation)
Family history of female breast cancer diagnosed before age 50	Family history of malignant neoplasm of breast at under age 50 in second degree female relative (situation)
Family history of genetic mutation for Lynch syndrome	Family history of genetic mutation for Lynch syndrome (situation)
Family history of localised scleroderma	Family history of localised scleroderma
Family history of localized scleroderma	Family history of localised scleroderma
Family history of scleroderma	Family history of scleroderma
Family therapy	Family therapy
Fasciotomy	Incision of fascia
Fast neutron teletherapy	Fast neutron therapy
Fastening	Fastening (physical object)
Fasting patient	Fasting
Fauces	Fauces structure
Fear of	Fear (finding)
Fear of body smells	A fear that may be due to personal sensitivity, negative associations or social conditioning where people are taught from a young age to avoid unpleasant odors. It is not excessive and does not lead to significant anxiety and does not interfere with the individual's daily life and activities.
Fear of confined spaces	Fear of enclosed spaces (finding)
Fear of darkness	Fear of the dark
Fear of falling	Fear of falling (finding)
Fear of high places	Fear of heights
Fear of own body odor	A fear that may be due to social situations, inability to maintain personal hygiene or specific health conditions. It is not excessive or irrational.
Fear of own body odour	A fear that may be due to social situations, inability to maintain personal hygiene or specific health conditions. It is not excessive or irrational.
Fear of spiders	A fear of spiders that may cause feelings of unease or dislike but is mild and manageable and doesn't typically interfere with daily life. Unlike arachnophobia which is a severe and debilitating condition that significantly impacts a person's life.
Fecal impaction in rectum	Fecal impaction of rectum (disorder)
Fecal impaction of rectum	Fecal impaction of rectum (disorder)
Feeling low	Depressed mood
Feels light headed	Lightheadedness (finding)
Female genital system	Structure of female genital system subdivision
Femoral hernia repair	Repair of femoral hernia
Femoral herniorrhaphy	Repair of femoral hernia
Femoral nerve lesion	Lesion of femoral nerve (disorder)
Femoral nerve lesions	Lesion of femoral nerve (disorder)
Ferret	Mustela putorius subspecies furo (organism)
Ferroportin disease	A rare disorder of iron metabolism and transport characterised by iron retention in macrophages (particularly of the liver and spleen), with a clinical picture of mild anaemia and elevated of serum ferritin levels. Ferroportin disease is distinct from haemochromatosis as it is not associated with high transferrin saturation or low hepcidin concentrations.
Ferrugination	Ferrugination
Fetal adenocarcinoma of lung	Fetal adenocarcinoma of lung
Fetal malpresentation	Malpresentation of fetus
Fetal membranes	Structure of amnion and/or chorion (body structure)
Fetal part	Fetal part
Fetoscopic examination of fetus	Fetoscopy
Fetus under 500gms	Structure of fetus under 500gms
Fiberoptic bronchoscope	Flexible fibreoptic bronchoscope
Fiberoptic bronchoscope	Fiberoptic bronchoscope
Fibreoptic bronchoscope	Flexible fibreoptic bronchoscope
Fibrillary gliosis	Fibrillary gliosis
Fibrinoid degeneration	Fibrinoid degeneration
Fibrinolysin, human	Human fibrinolysin (substance)
Fibroelastosis cordis	Congenital endocardial fibroelastosis (disorder)
Fibroepithelial hyperplasia	Mucous membrane hyperplasia
Fibroepithelial polyp of oral mucosa	Fibroepithelial polyp of oral mucous membrane (disorder)
Fibrosarcoma	Fibrosarcoma
Fibrosing alveolitis associated with rheumatoid arthritis	Rheumatoid fibrosing alveolitis
Fibrosis of pericardium	Fibrosis of pericardium
Fibrothecoma	Fibrothecoma
Fibrous corn	Fibrous corn (disorder)
Fibroxanthogranuloma	Xanthogranuloma (morphologic abnormality)
Fibroxanthogranuloma	Benign fibrous histiocytoma
Filter	Filter
Fimbria	Fimbria (cell structure)
Final cementation of crown to tooth	Fixation of crown to tooth using dental cement (procedure)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001166019	REFERS TO concept association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001167011	REFERS TO concept 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)