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1292992004: 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)

2698 members. Search Members:

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
ypT1c (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT1c1 (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT1c2 (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT1c3 (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT1d (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT1mi (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT2 (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT2a (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT2a1 (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT2a2 (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT2b (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT2c (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT2d (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT3 (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT3a (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT3b (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT3c (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT3d (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT4 (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT4a (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT4b (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT4c (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypT4d (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypT4e (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypTX (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypTa (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
ypTis (UICC) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypTis(DCIS) (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypTis(LAMN) (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypTis(LCIS) (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Union for International Cancer Control ypTis(Paget) (qualifier value) en Attribution Union for International Cancer Control: https://www.uicc.org/who-we-are/about-uicc/uicc-and-tnm
Upper limb defect with eye and ear abnormalities syndrome (disorder) en Attribution Inserm Orphanet
Uveal coloboma with cleft lip and palate and intellectual disability syndrome (disorder) en Attribution Inserm Orphanet
VPS11-related autosomal recessive hypomyelinating leukodystrophy en Attribution Inserm Orphanet
VEXAS syndrome en Attribution Inserm Orphanet
Ventilator-induced diaphragmatic dysfunction (disorder) en Attribution Inserm Orphanet
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus (disorder) en Attribution Inserm Orphanet
WT limb blood syndrome (disorder) en Attribution Inserm Orphanet
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder) en Attribution Inserm Orphanet
Waardenburg Shah syndrome en Attribution Inserm Orphanet
Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome (disorder) en Attribution Inserm Orphanet
Wasting syndrome due to acquired immunodeficiency syndrome (disorder) en Attribution Inserm Orphanet
Weismann Netter syndrome (disorder) en Attribution Inserm Orphanet
White platelet syndrome (disorder) en Attribution Inserm Orphanet
Witteveen Kolk syndrome en Attribution Inserm Orphanet
Wolf Hirschhorn syndrome (disorder) en Attribution Inserm Orphanet
X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder) en Attribution Inserm Orphanet
X-linked cone dysfunction syndrome with myopia (disorder) en Attribution Inserm Orphanet
X-linked corneal dermoid (disorder) en Attribution Inserm Orphanet
X-linked dominant erythropoietic protoporphyria en Attribution Inserm Orphanet
X-linked endothelial dystrophy of cornea (disorder) en Attribution Inserm Orphanet
X-linked epilepsy with learning disability and behavior disorder syndrome (disorder) en Attribution Inserm Orphanet
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (disorder) en Attribution Inserm Orphanet
X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability en Attribution Inserm Orphanet
X-linked intellectual disability Abidi type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Armfield type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Atkin type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Cantagrel type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Cilliers type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Miles Carpenter type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Pai type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Schimke type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Seemanova type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Shrimpton type en Attribution Inserm Orphanet
X-linked intellectual disability Siderius type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Stevenson type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Stocco Dos Santos type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Stoll type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Van Esch type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability Wilson type (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability with ataxia and apraxia syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) en Attribution Inserm Orphanet
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome en Attribution Inserm Orphanet
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome en Attribution Inserm Orphanet
X-linked intellectual disability, hypotonia, movement disorder syndrome en Attribution Inserm Orphanet
X-linked intellectual disability, short stature, overweight syndrome en Attribution Inserm Orphanet
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome en Attribution Inserm Orphanet
X-linked lissencephaly with abnormal genitalia syndrome en Attribution Inserm Orphanet
X-linked lymphoproliferative disease due to SH2D1A deficiency (disorder) en Attribution Inserm Orphanet
X-linked lymphoproliferative disease due to XIAP deficiency en Attribution Inserm Orphanet
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) en Attribution Inserm Orphanet
X-linked myotubular myopathy, abnormal genitalia syndrome (disorder) en Attribution Inserm Orphanet
X-linked neurodegenerative syndrome Bertini type (disorder) en Attribution Inserm Orphanet
X-linked neurodegenerative syndrome Hamel type (disorder) en Attribution Inserm Orphanet
X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) en Attribution Inserm Orphanet
X-linked retinal dysplasia (disorder) en Attribution Inserm Orphanet
X-linked severe congenital neutropenia (disorder) en Attribution Inserm Orphanet
XK aprosencephaly syndrome (disorder) en Attribution Inserm Orphanet
Xp21 deletion syndrome (disorder) en Attribution Inserm Orphanet
Xq25 microduplication syndrome en Attribution Inserm Orphanet
Young onset Parkinson disease (disorder) en Attribution Inserm Orphanet
Zellweger-like syndrome without peroxisomal anomaly (disorder) en Attribution Inserm Orphanet
NDE1-related microhydranencephaly en Attribution Inserm Orphanet

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Reference Sets

Reference set descriptor

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US English

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