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
Clear cell squamous cell carcinoma of trachea	Clear cell squamous cell carcinoma of trachea (disorder)
Clear lens extraction	Extraction of lens of eye (procedure)
Cleft soft palate, central	Central cleft of soft palate (disorder)
Clergy	Clergy
Clinical disease AND/OR syndrome present	Functional disease present
Clinical disease AND/OR syndrome present	Organic disease present
Clinically significant diabetic macular edema	Clinically significant macular edema due to diabetes mellitus
Clinically significant diabetic macular oedema	Clinically significant macular edema due to diabetes mellitus
Closed division of angle of mandible	Closed division of angle of mandible (procedure)
Closed reduction of dislocation of knee	Closed reduction of dislocation of knee
Clostridioides difficile gastrointestinal tract infection	Intestinal infection caused by Clostridioides difficile (disorder)
Clostridium difficile gastrointestinal tract infection	Intestinal infection caused by Clostridioides difficile (disorder)
Clostridium durum	Paenibacillus durus
Closure of oroantral communication	Closure of oroantral communication (procedure)
Clothing dishevelled	Clothing disheveled
Cobbler's chest	Pectus excavatum (disorder)
Cocaine delirium	Delirium caused by cocaine
Cocaine induced delirium	Delirium caused by cocaine
Cocaine-related disorder	Disorder caused by cocaine
Coccyx	Structure of coccygeal vertebral column
Coin lesion of lung	Coin lesion of lung
Colonic lavage via colostomy	Irrigation of colon via colostomy
Color vision deficiency	Color vision deficiency (disorder)
Colorectal cancer	Malignant neoplasm of cecum and/or colon and/or rectum (disorder)
Colour vision deficiency	Color vision deficiency (disorder)
Colporrhaphy	Repair of enterocele
Colporrhaphy for repair of rectocele	Posterior repair of vagina (procedure)
Colporrhaphy for repair of rectocoele	Posterior repair of vagina (procedure)
Columnar cell papilloma	Oncocytic Schneiderian papilloma of uncertain behavior (morphologic abnormality)
Comitant esophoria	A type of esophoria where the inward deviation is consistent in all directions of gaze.
Comitant heterophoria	A condition where the eyes have a tendency to drift out of alignment, which becomes noticeable only when binocular vision is disrupted. This misalignment is comitant, meaning the degree of deviation remains consistent across all gaze directions.
Comitant hypophoria	A vertical misalignment where one eye tends to move downward, only noticeable when binocular vision is disrupted such as when one eye is covered. The misalignment is the same in all directions of gaze.
Common variable immunodeficiency	Common variable immunodeficiency
Community dietitian	Community dietician (occupation)
Community-based dietitian	Community dietician (occupation)
Companion	Companion
Compartment syndrome of forearm	Compartment syndrome of forearm (disorder)
Compartment syndrome of forearm (disorder)	Compartment syndrome of forearm (disorder)
Complete color blindness	Complete achromatopsia
Complete colour blindness	Complete achromatopsia
Complete colpocleisis	Complete colpocleisis
Complete dislocation of tooth	Complete avulsion of tooth (disorder)
Complete edentulism	Edentulous
Complete hydatidiform mole	Benign complete hydatidiform mole
Complicated systemic gonorrhea	Disseminated infection caused by Neisseria gonorrhoeae (disorder)
Complicated systemic gonorrhoea	Disseminated infection caused by Neisseria gonorrhoeae (disorder)
Computed tomography enterography	Computed tomography of small intestine with contrast (procedure)
Computerised axial tomography of head	CT of head
Computerised axial tomography of thorax with contrast	CT of thorax with contrast
Computerised tomography of head	CT of head
Computerized axial tomography of head	CT of head
Computerized axial tomography of thorax with contrast	CT of thorax with contrast
Computerized tomography of head	CT of head
Concentration impairment	Impaired concentration (finding)
Concha nasalis	Nasal turbinate structure
Condensed milk	Condensed milk
Condyloma acuminatum	Anogenital warts (disorder)
Condylomata acuminatum	Anogenital warts (disorder)
Condylomatous carcinoma	Warty (condylomatous) carcinoma (morphologic abnormality)
Condylus lateralis humeri	Structure of lateral condyle of humerus (body structure)
Congenital abnormality of inner ear	Congenital anomaly of inner ear
Congenital absence of fallopian tube	Congenital absence of oviduct (disorder)
Congenital absence of liver,total	Agenesis of liver (disorder)
Congenital absence of oviduct	Congenital absence of oviduct (disorder)
Congenital absence of testis, unilateral	Absent testicle (congenital)
Congenital afibrinogenaemia	Congenital afibrinogenemia
Congenital afibrinogenemia	Congenital afibrinogenemia
Congenital anomaly of umbilical artery	Congenital anomaly of umbilical artery (disorder)
Congenital cardiovascular disorder	Congenital cardiovascular disorder (disorder)
Congenital common duct cyst	Congenital cystic dilatation of common bile duct
Congenital coronary arteriovenous fistula	Congenital coronary arteriovenous fistula (disorder)
Congenital crooked finger	Congenital clinodactyly of finger
Congenital cystic dilatation of common bile duct	Congenital choledochal cyst (disorder)
Congenital deformity of lower limb	Congenital deformity of lower limb (disorder)
Congenital deformity of musculoskeletal system	Congenital deformity of musculoskeletal system (disorder)
Congenital deformity of scapula	Congenital deformity of scapula (disorder)
Congenital discoid lateral meniscus	Congenital discoid lateral meniscus of knee (disorder)
Congenital endocardial fibroelastosis	Congenital endocardial fibroelastosis (disorder)
Congenital folate malabsorption	Congenital folate malabsorption anaemia
Congenital generalised fibromatosis	Infantile myofibromatosis
Congenital generalised fibromatosis	Congenital generalized fibromatosis (morphologic abnormality)
Congenital generalized fibromatosis	Congenital generalized fibromatosis (morphologic abnormality)
Congenital generalized fibromatosis	Infantile myofibromatosis
Congenital giant pigmented naevus	Pigmented nevus
Congenital giant pigmented nevus	Pigmented nevus
Congenital glottic web of larynx	Congenital glottic web of larynx
Congenital hydrocele of canal of Nuck	Congenital hydrocele of canal of Nuck (disorder)
Congenital hypofibrinogenaemia	Congenital hypofibrinogenemia (disorder)
Congenital hypofibrinogenemia	Congenital hypofibrinogenemia (disorder)
Congenital hypothyroidism	Congenital hypothyroidism
Congenital ichthyosis	Congenital ichthyosis of skin
Congenital iodine deficiency hypothyroidism	Congenital iodine deficiency syndrome
Congenital iodine deficiency syndrome	Congenital iodine deficiency syndrome
Congenital iodine deficiency syndrome - myxedematous type	Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)
Congenital iodine deficiency syndrome - myxoedematous type	Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)
Congenital lordosis due to bony malformation	Congenital lordosis deformity of spine due to congenital malformation of skeletal bone (disorder)
Congenital malformation due to valproic acid	Congenital malformation caused by valproic acid
Congenital malformation of inner ear	Congenital anomaly of inner ear
Congenital malformation of lens	Congenital anomaly of lens
Congenital megacalycosis	Congenital megacalycosis (disorder)
Congenital monosaccharide malabsorption	Congenital monosaccharide malabsorption

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Reference Sets

Reference set descriptor

Back to Start

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)