1292992004: Component annotation with string value reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Component annotation with string value reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2023. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

5276957018 Component annotation with string value reference set (foundation metadata concept) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

5276958011 Component annotation with string value reference set en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Component annotation with string value reference set (foundation metadata concept)	Is a	Reference set	true	Inferred relationship	Some

Members	languageDialectCode	typeId	value
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Transient infantile hypertriglyceridemia and hepatosteatosis is a rare, genetic, hepatic disease characterized by massive hepatomegaly, moderate to severe, transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis), manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fatty liver. Reduction or normalization of triglyceride serum levels occurs with advancing age.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Neonatal iodine exposure is a rare endocrine disease characterized by the appearance of transient hypothyroidism, usually in preterm newborns, following long or short-term topical iodine exposure. Parenteral exposure from iodinated contrast agents may similarly alter thyroid function in term neonates.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Transient neonatal multiple acyl-CoA dehydrogenase deficiency describes a very rare condition where a maternal riboflavin deficiency causes an infant to present with manifestations similar to those seen in multiple acyl-CoA dehydrogenase (MAD) deficiency such as poor suck, metabolic acidosis and hypoglycemia, but that resolves completely with oral riboflavin. In the one patient described haploinsufficiency of the human riboflavin transporter (hRFT1) was described in the mother.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare renal tubulopathy secondary to urinary tract infection (UTI) and/or urinary tract malformation (UTM) characterized by renal tubular resistance to aldosterone, characterized by hyponatremia, metabolic acidosis, hyperkalemia and inappropriately high serum aldosterone concentration and clinically manifesting as dehydration, vomiting, and poor oral intake.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare congenital disorder of glycosylation characterized by chronic, non-progressive liver disease, manifesting as mild steatosis with elevated serum transaminases and alkaline phosphatase, hypercholesterolemia, and decreased coagulation factors and ceruloplasmin. Transferrin glycosylation pattern is consistent with a type 2 congenital disorder of glycosylation. Liver biopsy may show mild non-progressive fibrosis. Patients usually remain asymptomatic, although delayed psychomotor development and hypotonia have been reported in single cases.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare, genetic, neurodevelopmental disorder characterized by global developmental delay, congenital heart defects, generalized hypertrichosis and dysmorphic facial features, most commonly triangular face, thick arched eyebrows, widely spaced eyes, posteriorly rotated low set ears, depressed nasal bridge, broad nasal root and tip, and pointed chin.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare genetic mandibulofacial dysostosis characterized by bilateral symmetrical oto-mandibular dysplasia including underdeveloped cheekbones (malar hypoplasia), a very small low jaw (micrognathia) and downward-slanting palpebral fissures, coloboma of the lower eyelids, microtia, hearing loss and without abnormalities of the extremities. Intelligence is normal.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Tremor-nystagmus-duodenal ulcer syndrome is a rare hyperkinetic movement disorder characterized by mild to severe, progressive essential tremor, nystagmus (principally horizontal), duodenal ulceration and a narcolepsy-like sleep disturbance. Refractive errors and cerebellar signs, such as gait ataxia and adiadochokinesia, may be associated. There have been no further descriptions in the literature since 1976.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trichodermodysplasia-dental alterations syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by sparse, thin, brittle scalp hair, as well as sparse eyebrows, eyelashes, axillary and pubic hair, delayed eruption of deciduous teeth and hypodontia of both dentitions. Mild palmoplantar keratosis, café-au-lait spots on back, mild dystrophy of nails, and tibial deflection of toes are also associated. There have been no further descriptions in the literature since 1986.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Virus-associated trichodysplasia spinulosa is a rare infectious skin disease characterized by the development of follicular papules with keratin spicules in various parts of the body, predominantly in the face (e.g. nose, eyebrows, auricles), that is due to polyomavirus infection in immunocompromized patients.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare ectodermal dysplasia syndrome characterized by the association of amelogenesis imperfecta and trichodysplasia with symmetrical pits in the cuticles of hair shafts. There have been no further descriptions in the literature since 1993.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trichodysplasia-xeroderma syndrome is an extremely rare, syndromic hair shaft anomaly characterized by sparse, coarse, brittle, excessively dry and slow-growing scalp hair, sparse axillary and pubic hair, sparse or absent eyelashes and eyebrows and dry skin. Hair shaft analysis shows pili torti, longitudinal splitting, grooves, peeling and scaling. There have been no further descriptions in the literature since 1987.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, also known as Oliver-McFarlane syndrome, is an extremely rare genetic disorder characterized by hair abnormalities, severe chorioretinal atrophy, hypopituitarism, short stature, and intellectual disability.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trichoodontoonychial dysplasia is a rare ectodermal dysplasia syndrome characterized by severe generalized hypotrichosis, parietal alopecia, secondary anodontia resulting from enamel hypoplasia, onychodystrophy, bone deficiency in the frontoparietal region and skin manifestations (including nevus pigmentosus, papules, ephelides, palmoplantar keratosis, supernumerary nipples, abnormal dermatoglyphics). There have been no further descriptions in the literature since 1983.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare multiple congenital anomalies syndrome characterized by short stature, sparse and depigmented scalp hair, typical facial characteristics (broad eyebrows, especially the medial portion, broad nasal ridge and tip, underdeveloped nasal alae, long philtrum, thin upper lip vermilion, and protruding ears), and limb anomalies (brachydactyly, short metacarpals and metatarsals, cone-shaped phalangeal epiphyses, dystrophic nails, and hip dysplasia).	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare, genetic, syndromic hair shaft abnormality disorder characterised by short, dry, sulphur-deficient, brittle hair usually associated with highly variable neuroectodermal manifestations, such as ichthyosis, photosensitivity, and intellectual disability.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
C syndrome is a rare multiple congenital anomaly/intellectual disability syndrome characterized by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare developmental defect during embryogenesis characterized by premature closure of metopic sutures and/or other sutures, short stature, and developmental delay. Dysmorphic features include trigonocephaly, metopic ridge, narrow forehead, bitemporal narrowing, arched eyebrows, hypotelorism, deep-set eyes, epicanthal folds, strabismus, wide nasal bridge, small pointed nose, anteverted nostrils, long philtrum, low-set ears, malar flattening, narrow mouth, thin lips, high-arched palate, crowded teeth, and micrognathia. Variable additional manifestations may include conductive hearing loss, cerebral (mainly involving the white matter), skeletal (e.g. brachymesophalangy of the fifth fingers), cardiovascular and renal anomalies, inguinal hernia, hypospadias, and seizures.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare developmental defect during embryogenesis characterized by unilateral duplication of an eye which may appear as a synophthalmic eye in a single orbit or as two separate unilateral eyes, each in a separate orbit. The malformation is always associated with other anomalies of the central nervous system (such as porencephaly, meningocele, or arachnoidal cysts) and with craniofacial abnormalities. A proboscis is often found. Clinically, moderate mental retardation and epilepsy are typical.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare genetic gastroenterological disease characterized by infantile or childhood onset of severe gastrointestinal inflammation. Patients present with a variable phenotype including fever, diarrhea, failure to thrive, oral ulcers, fistulating perianal disease, strictures, granulomatous colitis, and recurrent bacterial and viral infections.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare genetic syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy characterized by duplication anomalies such as triphalangeal thumbs, phalangeal duplication of other digits, and polydactyly, associated with highly variable combinations of ectrodactyly, brachydactyly, and syndactyly of hands and/or feet. Severe nail dysplasia or absence of nails is also observed.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trisomy 17p is a rare chromosomal abnormality resulting from the duplication of the short arm of chromosome 17 and characterized by pre- and post-natal growth retardation, developmental delay, hypotonia, digital abnormalities, congenital heart defects, and distinctive facial features.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trisomy 1q is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 1, with a highly variable phenotype principally characterized by intellectual disability, short stature, craniofacial dysmorphism (including macro/microcephaly, prominent forehead, posteriorly rotated, low-set ears, abnormal palpebral fissures, microphthalmia, broad, flat nasal bridge, high-arched palate, micro/retrognathia), cardiac defects and urogenital anomalies. Patients may also present cerebral (e.g. ventriculomegaly) and gastrointestinal malformations, as well as dystonic tremor and recurrent respiratory tract infections.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Trisomy 8p is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 8, with highly variable phenotype ranging from no dysmorphic features and only mild intellectual disability to patients with severe developmental delay, neonatal hypotonia, short stature, profound intellectual disability, mild dysmorphic features (e.g. mild ptosis, hypertelorism, down-slanting palpebral fissures, broad nasal bridge, short, prominent philtrum, abnormal dentition) and structural brain abnormalities. Autism, epilepsy, and spastic paraplegia have also been reported.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Tropical endomyocardial fibrosis is a restrictive cardiopathy, occurring almost exclusively in children and young adults in tropical and subtropical regions, characterized by endocardial fibrosis, affecting the apices and the inflow tract of the right or left ventricle (or both) and manifesting with a restrictive cardiomyopathy and atrioventricular regurgitation leading to severe pulmonary hypertension, very high systemic venous pressure and congestive cardiac failure. Suspected etiologies include helminth and protozoal infestation and malnutrition.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare congenital limb malformation with characteristics of true congenital dislocation of the shoulder, developing in utero. It can be unilateral or bilateral and is usually associated with other abnormalities of the shoulder girdle, such as in the glenoid, the humeral head, the joint capsule, and the scapula. In addition, it may be accompanied by other malformations, like developmental hip dysplasia or cardiac malformation.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare mitochondrial oxidative phosphorylation disorder characterized by a spectrum of three main clinical phenotypes comprising a severe neonatal phenotype with early fatal lactic acidosis, a more protracted course with early-onset developmental delay, motor weakness, extrapyramidal signs, with or without epilepsy, and a phenotype with normal early development and Parkinson-like symptoms starting around the age of one year. Additional, variably reported, signs and symptoms include cardiomyopathy, optic anomalies, hepatosplenomegaly, and abnormal brain MRI findings, among others. Deficiencies in mitochondrial oxidative phosphorylation enzymes are inconsistent.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare renal disease characterized by hypokalemic metabolic alkalosis secondary to a tubulopathy, hypomagnesemia with hypermagnesuria, severe hypercalciuria and dilated cardiomyopathy.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare genetic central nervous system malformation characterized by dysplasia of the superior cerebellum (especially the vermis), brainstem asymmetry, dysplasia of the basal ganglia, and cortical irregularities with asymmetric abnormalities in gyral size and orientation, as well as varying sulcal depth, but without lissencephaly, pachygyria, or polymicrogyria. Clinically, patients present global developmental delay with motor development usually being more affected that speech. Variable features are abnormal eye movements including oculomotor apraxia, strabismus, seizures, and behavioral problems.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay or regression, variable congenital heart defects (such as patent ductus arteriosus, atrial or ventricular septal defects, and double outlet right ventricle, among others), and dysmorphic features (including ptosis, epicanthal folds, abnormally set/dysplastic ears, low hairline or excess nuchal skin, wide-spaced/inverted nipples, umbilical hernia or diastasis recti, and digital anomalies). Additional variable manifestations are hyper- or hypotonia, seizures, hearing loss, cortical blindness, and optic atrophy. Brain imaging may show cerebral and cerebellar atrophy and hydrocephalus.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare genetic disease characterized by juvenile-onset insulin-dependent diabetes mellitus associated with central and peripheral nervous system abnormalities with variable onset between infancy and adolescence. Neurological manifestations include combined cerebellar and afferent ataxia, sensorineural hearing loss, pyramidal tract signs, and demyelinating sensorimotor peripheral neuropathy. Hypothyroidism has been reported in some patients. Brain imaging may show generalized cerebral atrophy.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Typical nemaline myopathy is a moderate neonatal form of nemaline myopathy characterized by facial and skeletal muscle weakness and mild respiratory involvement.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare genetic neurological disorder characterized by severe pseudo-TORCH syndrome with signs of brain damage and occasionally systemic manifestations resembling the sequelae of congenital infection, but in the absence of an infectious agent. Characteristic features include microcephaly, white matter disease, cerebral atrophy, cerebral hemorrhage, and calcifications, among others. Affected individuals typically have seizures and respiratory insufficiency and die in infancy.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare syndromic intestinal malformation characterized by ulcer formation in the umbilical cord associated with congenital upper-intestinal atresia, typically presenting with intra-uterine hemorrhaging from the ulcer site and subsequent fetal bradycardia.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare congenital malformation syndrome characterized by ulnar hypoplasia associated with hypoplastic to absent fourth and/or fifth digits, fibular hypoplasia, short stature and facial dysmorphism.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Unclassified myelodysplastic syndrome (MDS-U) is a subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Tricho-retino-dento-digital syndrome is an autosomal dominant ectodermal dysplasia syndrome, characterized by uncombable hair syndrome, congenital hypotrichosis and dental abnormalities such as oligodontia or hyperdontia, and associated with early-onset cataract, retinal pigmentary dystrophy, and brachydactyly with brachymetacarpia. Furthermore, hyperactivity and a mild intellectual deficit have been reported in affected patients.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare type of pancreatic ductal adenocarcinoma characterized by composition of non-neoplastic osteoclast-like multinucleated giant cells, a mononuclear histiocytic component, and the neoplastic cells, which vary from spindle-shaped to epithelioid and can be very large and pleomorphic. Clinical features of pancreatic ductal adenocarcinoma include abdominal pain, nausea, weight loss, jaundice, and new-onset diabetes.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
A rare hematological neoplasm characterized by clonal proliferation of myeloid precursors in the bone marrow, blood and other tissues (spleen, liver), with clinical, morphological and molecular features of myeloproliferative neoplasms (MPN), failing to meet criteria of a specific MPN. The presentation is nonspecific and variable and often includes leukocytosis, thrombocytosis and anemia. Splenomegaly, hepatomegaly as well as fatigue, malaise or weight loss may appear in advanced stages.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Unilateral polymicrogyria is a cerebral cortical malformation characterized by unilateral excessive cortical folding and abnormal cortical layering. It comprises two sub-types depending on the areas affected: unilateral hemispheric and focal polymicrogyria.	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Inserm Orphanet
Union for International Cancer Control R0 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control R1 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
R2 (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
RX (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control allowable value	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM0 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM0(i+) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cM0(mol+) (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1a (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1a(0) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cM1a(1) (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1b (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cM1b(0) (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1b(1) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cM1c (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1c(0) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1c(1) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1d (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cM1d(0) (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cM1d(1) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN0(i+) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN0(sn) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN1(sn) (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN1a (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN1a(sn) (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN1b (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN1c (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN1mi (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN2 (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN2a (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN2b (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN2c (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN2mi (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN3 (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN3a (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cN3b (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cN3c (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cNX (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cNX(sn) (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT0 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cT1a (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1a1 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1a2 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cT1b (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1b1 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1b2 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1b3 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1c (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cT1c1 (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1c2 (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cT1c3 (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control cT1d (qualifier value)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cT1mi (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
cT2 (UICC)	en	Attributed to a particular organization or group that contributes content to SNOMED CT.	Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
5276957018	Component annotation with string value reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
5276958011	Component annotation with string value reference set	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)