Members |
languageDialectCode |
typeId |
value |
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 |
UMOD-related autosomal dominant tubulointerstitial kidney disease |
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 |
Van den Bosch syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Van den Ende-Gupta syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Vasculitis due to adenosine deaminase 2 deficiency |
en |
Attribution |
Inserm Orphanet |
Vasculitis due to and following viral infection (disorder) |
en |
Attribution |
Inserm Orphanet |
Velofacioskeletal syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Ventilator-induced diaphragmatic dysfunction (disorder) |
en |
Attribution |
Inserm Orphanet |
Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Verloove Vanhorick Brubakk syndrome |
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 |
Vici syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (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 |
Weaver Williams syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Weismann Netter syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
White fibrous papulosis of neck |
en |
Attribution |
Inserm Orphanet |
White forelock with malformations syndrome |
en |
Attribution |
Inserm Orphanet |
White platelet syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Wiedemann Steiner syndrome |
en |
Attribution |
Inserm Orphanet |
Wilson Turner syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Witteveen Kolk syndrome |
en |
Attribution |
Inserm Orphanet |
Wolf Hirschhorn syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Wolfram-like syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome |
en |
Attribution |
Inserm Orphanet |
Wooly hair with palmoplantar keratoderma syndrome |
en |
Attribution |
Inserm Orphanet |
X-linked Charcot-Marie-Tooth disease type 1 |
en |
Attribution |
Inserm Orphanet |
X-linked Charcot-Marie-Tooth disease type 2 (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked Charcot-Marie-Tooth disease type 3 |
en |
Attribution |
Inserm Orphanet |
X-linked Charcot-Marie-Tooth disease type 4 |
en |
Attribution |
Inserm Orphanet |
X-linked Charcot-Marie-Tooth disease type 5 (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked Charcot-Marie-Tooth disease type 6 (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 cerebral, cerebellar, coloboma syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked cleft palate and ankyloglossia |
en |
Attribution |
Inserm Orphanet |
X-linked cone dysfunction syndrome with myopia (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked corneal dermoid (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked diffuse leiomyomatosis with Alport syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked distal arthrogryposis multiplex congenita (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked distal spinal muscular atrophy type 3 (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked dominant chondrodysplasia Chassaing Lacombe type (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 hereditary sensory and autonomic neuropathy with deafness (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked immunoneurologic disorder (disorder) |
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 Cabezas 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 Hedera type (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked intellectual disability Miles Carpenter type (disorder) |
en |
Attribution |
Inserm Orphanet |
X-linked intellectual disability Nascimento 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 acromegaly and hyperactivity 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 |