Catalogue of samples from Vall d'Hebron University Hospital Biobank Use the search engine to find the samples you need for your research. Disease group - Any -Cardiovascular diseaseDigestive diseaseDisease group categoryGestational diseaseImmune diseaseInfectious DiseaseKidney diseaseNeurological and/or Psychiatric diseaseOncological diseasePaediatric diseaseRare diseaseRespiratory disease Sample type - Any -BloodBuffy coatCerebrospinal fluidDNAFibroblastsPBMCsPlasmaRNASerumStoolTissue (frozen)Type of sampleUrine Diagnosis - Any -A20 deficiency (TNFAIP3)ADA DeficiencyAgammaglobulinemia of unknown cause or unlisted gene defectAID deficiency (AICDA)ALPS-Caspase 10ALPS-FASALPS-FAS (TNFRSF6)Alteration in sex determination or differentiationAmyotrophic lateral sclerosisAnencephalyAPECED (APS-1), autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (AIRE)ARPC1B deficiency (ARPC1B)Arterial hypertentionAtaxia– telangiectasiaAutosomal recessive CGD – p47 phox deficiency (NCF1)Bladder cancerBowel cancerBrain aneurysmBrain cancerBreast cancerBreast cancer with cardiotoxicityBTK deficiencyCatastrophic antiphospholipid syndromeCD40L deficiency (CD40LG)Cerebrovascular diseaseChronic Functional DiarrheaChronic Granulomatous Disease (CGD)Chronic granulomatous disease, p47 phox deficiency (NCF1)Chronic granulomatous disease, X-linked gp91 phox deficiency (CYBB)Chronic ischaemic colitisChronic kidney disease, stage 2 (mild)Chronic mucocutaneous candidiasisCollagenous colitisColon cancerCommon variable immunodeficiency disordersComplete Trisomy withouth mosaicism Congenital malformations of the circulatory system groupControl (cardiovascular disease) Control (infectious disease)Control (organ donor)Control Frozen fetal tissue samplesCOVID-19Crohn's diseaseCTLA4 deficiencyCYSTIC FIBROSISDiabetes mellitus type 1Diabetes mellitus type 2Diagnosis: ICD-10 text description (eg: Lymphocytic colitis)Diarrhea-predominant irritable bowel syndrome (IBS-D)DiGeorge syndromeDOCK8 deficiencyEDA-ID, X-linked (NEMO deficiency)Endometrial and uterine cancerEsophagus cancerFactor I deficiencyFamilial Mediterranean Fever (MEFV)Gastric cancerGATA2 deficiencyGc deficiencyGc deficiency (IL2RG)Gestational diabetesGlioblastomaGriscelli syndromeGrowth retardationHealthy subject (cardiovascular disease control)Healthy subjects (microscopic colitis control)Herpetic EncephalitisHLH with unknown or unlisted genetic causeHyper IgE syndrome AD STAT3 (STAT3)Hypertension (arterial hypertension resistant to antihypertensives treatment)Hypogammaglobulinemia of unknown causeHypogammaglobulinemia of unknown cause or uniisted gene defectIgA with IgG subclass deficiencyImmunodeficiency under study (not classified)Incomplete lymphocytic colitisInfection due to enterovirus, unspecifiedIPEX (FoxP3)JAK3 deficiencyKabuki syndromeKidney cancerKidney trasplantedLaryngeal cancerLeukocyte adhesion deficiency type 1 (LAD1) (ITGB2)Lewy body diseaseLiver cancerLoeys-Dietz syndromeLRBA deficiency (LRBA)Lung cancerLung cancer with brain metastasisLung trasplantedLymphocytic colitisMarfan syndromeMassive tau-positive astrogliopathy (AT8)Myocardial infarctionNBAS deficiencyNephrotic syndrome with membranous glomerulonephritisNephrotic syndrome with minor glomerular anomalyNephrotic syndrome with unspecified morphological alterationsNFKB1 deficiency (NFKB1)Non-syndromic familial thoracic aortic aneurysms and dissectionsObesity and Diabetes mellitus type 2Omenn syndromeOral cavity cancerOther_Autoinflammatory disordersOther_Combined immunodeficienciesOther_Combined immunodeficiencies with associated or syndromic featuresOther_Congenital defects of phagocytesOther_Defectes in innate immunityOther_Defects in innate immunityOther_Diseases of immune dysregulationOther_Predominantly antibody deficienciesOvarian cancerPancreatic cancerParkinson diseasePerforin deficiencyPI3 Kinase deficiencyPID under studyPLAID (PLCg2 associated antibody deficiency and immune dysregulation) (PLCG2)Progressive multifocal leukoencephalopathyPropuesta de buscador:Prostate CancerPsoriasic arthritisPsoriasisPurine nucleoside phosphorylase (PNP)RAG 2 deficiency (RAG2)Renal agenesisRheumatoid arthritisSCID unknown typeSecondary malignant neoplasia of lymph nodesSelective IgA deficiencySepsisSevere Combined Immunodeficiency (SCID)Shwachman-Diamond syndrome (SBDS)Síndrome de JacobsenSkin cancerSoft tissue cancerSpecific antibody deficiency with normal Ig concentrations and normal numbers of B cellsSTAT1 gain-of-function (STAT1)STING-SAVISystemic Inflammatory Response SyndromeSystemic lupus erythematosusTACI deficiencyThreatened preterm laborThyroid cancerTLR3 deficiency (TLR3)TNF receptor-associated periodic syndrome (TRAPS)Trisomy 13Trisomy 18Trisomy 21Uterine cancerVaginal cancerWiskott-Aldrich syndrome (WAS)X-linked chronic granulomatous disease (CGD)XIAP deficiency (XLP2) (XIAP)(BIRC4) ICD-10 code - Any -A40A41A81.2B00.4B34.1C00C01C02C03C04C05C06C07C08C09C10C11C12C13C14C15C16C17C18C22C25C30C33C34C43C44C50C52C53C54C56C61C64C67C71C71.9C73C81C82C83C84C85C86C87C88D61.0D68.8D71D76.1D80D80.0D80.1D80.2D80.3D80.5D80.6D80.9D81.1D81.2D81.3D81.9D82D82.0D82.1D82.3D82.4D82.9D83.0D83.1D84D84.1D84.8D84.9D89D89.9E10E11E66.9E84G05.1G11.3G12.2G20G31.8I10I11I12I13I15I21I22I60I61I62I63I64I65I66I67I67.2I68I69I71.2ICD0K50K52.3K52.831K52.832K55.9K58K59.1L40L40.5M05M06M07M32MUESTRASN04.0N04.2N04.9N18.2O24O60.1Q00Q01Q02Q03Q04Q05Q06Q07Q08Q09Q20Q21Q22Q23Q24Q25Q26Q27Q28Q60Q61Q62Q63Q64Q87.0Q87.4Q90Q91.0Q91.1Q91.2Q91.3Q91.4Q91.5Q91.6Q91.7Q92Q93Q93.5Q94Q95Q96Q97Q98Q99R65U07.1Z94.0Z94.2 ORPHA code - Any -282379558586811870193060030913879853499842103920140989293848 0 results found Sample request If you are interested in requesting samples, you can fill out the Sample request document and send it to the email: biobanc@vhir.org. This catalog is updated regularly. If you don't find what you need contact us biobanc@vhir.org. If Vall d'Hebron University Hospital Biobank does not have the sample you are looking for, you can contact to ISCIII Biobanks and Biomodels Platform European Biobank Network BBMRI-ERIC
