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 diseaseGestational diseaseImmune diseaseInfectious DiseaseKidney diseaseNeurological and/or Psychiatric diseaseOncological diseasePaediatric diseaseRare diseaseRespiratory disease Sample type - Any -BloodBuffy coatCerebrospinal fluidDNAFibroblastsPBMCsPlasmaRNASerumStoolTissue (frozen)Urine Diagnosis - Any -A20 deficiency (TNFAIP3)ADA DeficiencyAID deficiency (AICDA)ALPS-Caspase 10ALPS-FASALPS-FAS (TNFRSF6)APECED (APS-1), autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (AIRE)ARPC1B deficiency (ARPC1B)Agammaglobulinemia of unknown cause or unlisted gene defectAlteration in sex determination or differentiationAmyotrophic lateral sclerosisArterial hypertentionAtaxia– telangiectasiaAutosomal recessive CGD – p47 phox deficiency (NCF1)BTK deficiencyBladder cancerBowel cancerBrain aneurysmBrain cancerBreast cancerBreast cancer with cardiotoxicityCD40L deficiency (CD40LG)COVID-19CTLA4 deficiencyCYSTIC FIBROSISCatastrophic antiphospholipid syndromeCerebrovascular diseaseChronic Functional DiarrheaChronic Granulomatous Disease (CGD)Chronic granulomatous disease, X-linked gp91 phox deficiency (CYBB)Chronic granulomatous disease, p47 phox deficiency (NCF1)Chronic kidney disease, stage 2 (mild)Chronic mucocutaneous candidiasisChronic ischaemic colitisCollagenous colitisColon cancerCommon variable immunodeficiency disordersComplete Trisomy withouth mosaicism Congenital malformations of the circulatory system groupCongenital malformations of the nervous systemControl (cardiovascular disease) Control (infectious disease)Control (organ donor)Control Frozen fetal tissue samplesCrohn's diseaseDOCK8 deficiencyDiGeorge syndromeDiabetes mellitus type 1Diabetes mellitus type 2Diarrhea-predominant irritable bowel syndrome (IBS-D)EDA-ID, X-linked (NEMO deficiency)Endometrial and uterine cancerEsophagus cancerFactor I deficiencyFamilial Mediterranean Fever (MEFV)GATA2 deficiencyGastric cancerGc deficiencyGc deficiency (IL2RG)Gestational diabetesGlioblastomaGriscelli syndromeGrowth retardationHLH with unknown or unlisted genetic causeHealthy subject (cardiovascular disease control)Healthy subjects (microscopic colitis control)Herpetic EncephalitisHyper IgE syndrome AD STAT3 (STAT3)Hypertension (arterial hypertension resistant to antihypertensives treatment)Hypogammaglobulinemia of unknown causeHypogammaglobulinemia of unknown cause or uniisted gene defectIPEX (FoxP3)IgA with IgG subclass deficiencyImmunodeficiency under study (not classified)Incomplete lymphocytic colitisInfection due to enterovirus, unspecifiedJAK3 deficiencyKabuki syndromeKidney cancerKidney trasplantedLRBA deficiency (LRBA)Laryngeal cancerLeukocyte adhesion deficiency type 1 (LAD1) (ITGB2)Lewy body diseaseLiver cancerLoeys-Dietz syndromeLung cancerLung cancer with brain metastasisLung trasplantedLymphocytic colitisMarfan syndromeMassive tau-positive astrogliopathy (AT8)Myocardial infarctionNBAS deficiencyNFKB1 deficiency (NFKB1)Nephrotic syndrome with membranous glomerulonephritisNephrotic syndrome with minor glomerular anomalyNephrotic syndrome with unspecified morphological alterationsNon-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 cancerPI3 Kinase deficiencyPID under studyPLAID (PLCg2 associated antibody deficiency and immune dysregulation) (PLCG2)Pancreatic cancerParkinson diseasePerforin deficiencyProgressive multifocal leukoencephalopathyProstate CancerPsoriasic arthritisPsoriasisPurine nucleoside phosphorylase (PNP)RAG 2 deficiency (RAG2)Renal agenesisRheumatoid arthritisSCID unknown typeSTAT1 gain-of-function (STAT1)STING-SAVISecondary malignant neoplasia of lymph nodesSelective IgA deficiencySepsisSevere Combined Immunodeficiency (SCID)Shwachman-Diamond syndrome (SBDS)Skin cancerSoft tissue cancerSpecific antibody deficiency with normal Ig concentrations and normal numbers of B cellsSystemic Inflammatory Response SyndromeSystemic lupus erythematosusSíndrome de JacobsenTACI deficiencyTLR3 deficiency (TLR3)TNF receptor-associated periodic syndrome (TRAPS)Threatened preterm laborThyroid cancerTrisomy 13Trisomy 18Trisomy 21Uterine cancerVaginal cancerWiskott-Aldrich syndrome (WAS)X-linked chronic granulomatous disease (CGD)XIAP deficiency (XLP2) (XIAP)(BIRC4) ICD-10 code - Any -A40A41A81.2B00.4B34.1C00C01C02C03C04C05C06C07C08C09C10C11C12C13C14C15C16C17C18C22C25C30C33C34C43C44C50C52C53C54C56C61C64C67C71C71.9C73C81C82C83C84C85C86C87C88D61.0D68.8D71D76.1D80D80.0D80.1D80.2D80.3D80.5D80.6D80.9D81.1D81.2D81.3D81.9D82D82.0D82.1D82.3D82.4D82.9D83.0D83.1D84D84.1D84.8D84.9D89D89.9E10E11E66.9E84G05.1G11.3G12.2G20G31.8I10I11I12I13I15I21I22I60I61I62I63I64I65I66I67I67.2I68I69I71.2K50K52.3K52.831K52.832K55.9K58K59.1L40L40.5M05M06M07M32N04.0N04.2N04.9N18.2O24O60.1Q00Q01Q02Q03Q04Q05Q06Q07Q08Q09Q20Q21Q22Q23Q24Q25Q26Q27Q28Q60Q61Q62Q63Q64Q87.0Q87.4Q90Q91.0Q91.1Q91.2Q91.3Q91.4Q91.5Q91.6Q91.7Q92Q93Q93.5Q94Q95Q96Q97Q98Q99R65U07.1Z94.0Z94.2 ORPHA code - Any -282379558586811870193060030913879853499842103920140989293848 65,609 results found Stool 72 Tissue (frozen) 7,077 Serum 6,224 Plasma 10,661 Buffy coat 25 DNA 9,071 PBMCs 8,028 Fibroblasts 7 Urine 8,042 RNA 7,622 Blood 8,765 Cerebrospinal fluid 15 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
