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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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TissGeneSummary

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TissGeneExp

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TissGene-miRNA

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TissGeneMut: TissGeneSNV, TissGeneCNV, and TissGeneFusions

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TissGeneNet

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TissGeneProg

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TissGeneClin: TissGeneDrug and TissGeneDisease

TissGeneSummary for CASR
check button Gene summary
Basic gene informationGene symbolCASR
Gene namecalcium-sensing receptor
SynonymsCAR|EIG8|FHH|FIH|GPRC2A|HHC|HHC1|HYPOC1|NSHPT|PCAR1
CytomapUCSC genome browser: 3q13
Type of geneprotein-coding
RefGenesNM_000388.3,
NM_001178065.1,
Descriptionextracellular calcium-sensing receptorparathyroid Ca(2+)-sensing receptor 1parathyroid cell calcium-sensing receptor 1
Modification date20141222
dbXrefs MIM : 601199
HGNC : HGNC
Ensembl : ENSG00000036828
HPRD : 03122
Vega : OTTHUMG00000159491
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_CASR
BioGPS: 846
PathwayNCI Pathway Interaction Database: CASR
KEGG: CASR
REACTOME: CASR
Pathway Commons: CASR
ContextiHOP: CASR
ligand binding site mutation search in PubMed: CASR
UCL Cancer Institute: CASR
Assigned class in TissGDB*C
Included tissue-specific gene expression resourcesTiGER,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Kidney
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)KIRC,KIRP,KICH
Reference showing the relevant tissue of CASR
Description by TissGene annotationsHave significant anti-correlated miRNA
* Class A consists of genes with literature evidence and is part of the cTissGenes. Class B consists of only cTissGenes without additional evidence. The remaining genes belong to Class C.

check button Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO termPubMed ID
GO:0070509calcium ion import20846291
GO:0070509calcium ion import20846291


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TissGeneExp for CASR

check button Gene expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
gene exp


check button Gene isoform expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01)
gene isoform exp


check button Gene expressions across normal tissues of GTEx data
(GTEx GTEx_Analysis_v6_RNA-seq_RNA-SeQCv1.1.8_gene_rpkm.gct)
- Here, we shows the matched tissue types only among our 28 cancer types.
normal gene exp


check button Different expressions across 14 cancer types with more than 10 samples between matched tumors and normals (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
DEG exp

- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05)
Cancer typeMean(exp) in tumorMean(exp) in matched normalLog2FCP-val.FDR
KIRC1.1793478198.20265893-7.0233111113.28E-369.42E-35
KIRP1.6168474728.363869347-6.7470218752.38E-168.75E-15
KICH2.5326145978.336606597-5.8039924.46E-103.07E-09
COAD-2.2180147880.208096751-2.4261115381.15E-101.63E-09
LIHC-1.5944734031.426196597-3.020673.66E-151.10E-13
STAD-1.458593153-0.099677528-1.3589156250.009260.032438847
THCA-2.374252793-1.311151098-1.0631016950.000290.000742266


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TissGene-miRNA for CASR

check button Significantly anti-correlated miRNAs of TissGene across 28 cancer types
(Gene-miRNA relations from TargetScanHuman Relsease 7.1, Conserved_Site_Context_Scores.txt.zip, 06.01.2016)
(TCGA IlluminaHiSeq_miRNASeq, log2(RPM+1) data, version 2016-11-21)
(TCGA IlluminaHiSeq_RNASeqV2, log2(normalized_count+1) data, version 2016-08-16)
(Spearman’s Rank Correlation (p-value<0.05 and coefficient<-0.25))
Cancer typemiRNA idmiRNA accessionP-val.Coeff.# samples
ACChsa-miR-6838-5pMIMAT00275780.016-0.2978
ACChsa-miR-6838-5pMIMAT00275780.016-0.2978
LUADhsa-miR-429MIMAT00015360.0094-0.3460


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TissGeneMut for CASR
TissGeneSNV for CASR

check button nsSNV counts per each loci.
Different colors of circles represent different cancer types. Circle size denotes number of samples.
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)

* Click on the image to enlarge it in a new window.
SNV lollipop
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check button Somatic nucleotide variants of TissGene across 28 cancer types
(X-axis: cancer type and Y-axis: % of mutated samples)
The numbers in parentheses are numbers of samples with mutation (nsSNVs).
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)
SNV distribution

- nsSNVs sorted by frequency.
AAchangeCancer type# samples
p.P39SSKCM4
p.R392*STAD2
p.S923FSKCM2
p.S122YUCEC2
p.D500NSKCM2
p.G518ESKCM2
p.E582KSKCM2
p.E931KSKCM2
p.F629SSKCM2
p.R392QSKCM2
p.F619SSKCM2
p.E353KSKCM2
p.S490FSKCM2
p.A86VTHYM1
p.R227*STAD1
p.D585NSKCM1
p.P579LSKCM1
p.L360FSKCM1
p.L1025MLGG1
p.E241VLIHC1
p.E765*LUAD1
p.Q1027LLUAD1
p.G730RSKCM1
p.R886QBRCA1
p.S296RSKCM1
p.E582VSKCM1
p.G290SSKCM1
p.L770ILUAD1
p.L912VLUSC1
p.V653IPRAD1
p.S913FSKCM1
p.E1039KHNSC1
p.R331QMESO1
p.E332KSKCM1
p.T92KKIRP1
p.T972MSTAD1
p.R392XSTAD1
p.T406SBLCA1
p.G1029ESKCM1
p.R896CCOAD1
p.P569LSKCM1
p.G979DACC1
p.A880TUCEC1
p.A986SCOAD1
p.L689MUCEC1
p.S1061NLUAD1
p.G94EBLCA1
p.R561KSKCM1
p.R896WGBM1
p.G971SSTAD1
p.P692LPAAD1
p.R340SOV1
p.R688HOV1
p.E880VTHYM1
p.I491VLIHC1
p.E564KSKCM1
p.G567ESKCM1
p.P163SLUSC1
p.I613TLUSC1
p.E297KCESC1
p.F128LSTAD1
p.D1015NSKCM1
p.P89SSKCM1
p.G43ESKCM1
p.G21RHNSC1
p.P1015LUCEC1
p.E981KLUAD1
p.P757LSKCM1
p.E80KBRCA1
p.E614KLGG1
p.P935SCOAD1
p.R701LUCEC1
p.R69CUCEC1
p.G1034ESKCM1
p.L1035MLGG1
p.R185XSKCM1
p.Y514CSTAD1
p.W206XSKCM1
p.F615LLIHC1
p.N710KLUAD1
p.N583DSKCM1
p.E362KSKCM1
p.P711LPAAD1
p.A625TPAAD1
p.R711LLUAD1
p.R185*SKCM1
p.D1022NSKCM1
p.S342FSKCM1
p.R883CSARC1
p.R205CUCEC1
p.S830FSKCM1
p.G559RSKCM1
p.R227*UCEC1
p.P808LGBM1
p.G447SLIHC1
p.D31NSTAD1
p.W685*SKCM1
p.Q1017LLUAD1
p.P439TGBM1
p.K803EHNSC1
p.R392QSTAD1
p.E991KLUAD1
p.F183YLUSC1
p.Q764HLUAD1
p.K892QUCS1
p.E456KSKCM1
p.P393SSKCM1
p.D1032NSKCM1
p.P569SSKCM1
p.E574KSKCM1
p.D23NLUSC1
p.G695DSKCM1
p.E127*ACC1
p.E777KCESC1
p.G917ESKCM1
p.G903RSKCM1
p.R205HSTAD1
p.E350VLUSC1
p.P747LSKCM1
p.R906CDLBC1
p.H344LBRCA1
p.E809QESCA1
p.F76CUCEC1
p.E282DCESC1
p.A897GLUAD1
p.D1005NBRCA1
p.T186ISTAD1
p.D575NSKCM1
p.R726HDLBC1
p.Q432XSTAD1
p.E379KSKCM1
p.D23NSKCM1
p.V689MCOAD1
p.G366RSKCM1
p.G913RSKCM1
p.C851GSKCM1
p.R415QLIHC1
p.P163SSKCM1
p.L276FSKCM1
p.V894IBRCA1
p.A430VREAD1
p.P22LSKCM1
p.V1066MLUAD1
p.N593DSKCM1
p.A693TSTAD1
p.W728*SKCM1
p.G440RHNSC1
p.P923LCOAD1
p.R648CSKCM1
p.F320LESCA1
p.S171GLUSC1
p.M197ISKCM1
p.S388LSKCM1
p.R185QSKCM1
p.P1062SSKCM1
p.I613FSKCM1
p.V1056MLUAD1
p.N639KBRCA1
p.W828LPRAD1
p.N700KLUAD1
p.R701CSKCM1
p.P748SSKCM1
p.E871KSKCM1
p.A194VLUAD1
p.R701LLUAD1
p.P758SSKCM1
p.D990HLUSC1
p.E1030KSKCM1
p.D248HBLCA1
p.G969DACC1
p.F798YKIRC1
p.D398NLUAD1
p.K28NSKCM1
p.R69HLUSC1
p.R535MCOAD1
p.R205CESCA1
p.R901PLUSC1
p.D217NHNSC1
p.N732ILUAD1
p.A824TCOAD1
p.T151KLUAD1
p.R415WTHYM1
p.P920TUCEC1
p.S1071NLUAD1
p.R726CSARC1
p.L780ILUAD1
p.S697GSTAD1
p.V827IGBM1
p.S387NSKCM1
p.S687GSTAD1
p.T722IKIRC1
p.S417FSKCM1
p.E604KLGG1
p.S490FREAD1
p.L700FSTAD1
p.G567RSKCM1
p.L10IUCEC1
p.G581RSKCM1
p.R795QUCEC1
p.E1029KHNSC1
p.G30RSKCM1
p.R227XSTAD1
p.R901GLUSC1
p.C585FOV1
p.P596QLUAD1
p.V631MPAAD1
p.G768CHNSC1
p.T919SLUAD1
p.W206*SKCM1
p.P1045AHNSC1
p.D248NBLCA1
p.S303FSKCM1
p.E881KSKCM1
p.R901CLIHC1
p.E475DOV1
p.G685DSKCM1
p.A73VSKCM1
p.A589TLUAD1
p.Q968KPRAD1
p.P579SSKCM1
p.T92MCOAD1
p.E232GUCEC1
p.R96KSKCM1
p.G778CHNSC1
p.T92MLUAD1
p.P833SSKCM1
p.L665FSKCM1
p.S497FSKCM1
p.R285WUCEC1
p.P393LSKCM1
p.L184FSKCM1
p.K719NSTAD1
p.E1020KSKCM1
p.P721LPAAD1
p.W675XSKCM1
p.Q432*STAD1
p.L679MUCEC1
p.G1076RBLCA1
p.E777KSKCM1
p.R890HSTAD1
p.E620KSKCM1
p.A794SCESC1
p.L628FSKCM1
p.I813VUCEC1
p.T732ABRCA1
p.R890HPAAD1
p.R638CSKCM1
p.E767KUCEC1
p.E1053KHNSC1
p.V1081DLUAD1
p.G1044ESKCM1
p.V846LLUAD1
p.G376DLIHC1
p.R415WUCEC1
p.G363CLUAD1
p.P935LCOAD1
p.E681KSKCM1
p.F979SUCEC1
p.A579TLUAD1
p.G329SSKCM1
p.N1006TUCEC1
p.P910TUCEC1
p.S244FSKCM1
p.V846ISKCM1
p.I162MCOAD1
p.R66HOV1
p.G1066RBLCA1
p.E809KSKCM1
p.R906HBLCA1
p.R891HUCEC1
p.R711CSKCM1
p.C861GSKCM1
p.T898MPRAD1
p.K709NSTAD1
p.A430TKIRC1
p.E350KSKCM1
p.L618FSKCM1
p.K806*SKCM1
p.A295SLUAD1
p.Q260RSKCM1
p.P682LCOAD1
p.E1009KSKCM1
p.G30ESKCM1


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TissGeneCNV for CASR

check button Copy number variations of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of CNV samples)
(TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16)
CNV


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TissGeneFusions for CASR

check button Fusion genes including TissGene
(ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01)
DatabaseSrcCancer typeSampleFusion geneORF5'-gene BP3'-gene BP
Chimerdb3.0FusionScanLUADTCGA-91-8499-01AFAM162A-CASROut-of-Framechr3:122103146chr3:121980374
TCGAfusionPortalPRADABRCATCGA-D8-A27V-01ASUCLA2-CASR5UTR-5UTRChr13:48611742Chr3:121972795
TCGAfusionPortalPRADALUADTCGA-91-8499-01AFAM162A-CASROut-of-frameChr3:122103146Chr3:121980375
TCGAfusionPortalPRADAOVTCGA-23-1120-01ALPP-CASRIn-frameChr3:188202492Chr3:121980375


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TissGeneNet for CASR

check button Co-expressed gene networks based on protein-protein interaction data (CePIN)
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(PINA2 ppi data)
BRCA (tumor)BRCA (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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COAD (tumor)COAD (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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HNSC (tumor)HNSC (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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KICH (tumor)KICH (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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KIRC (tumor)KIRC (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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KIRP (tumor)KIRP (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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LIHC (tumor)LIHC (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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LUAD (tumor)LUAD (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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LUSC (tumor)LUSC (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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PRAD (tumor)PRAD (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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STAD (tumor)STAD (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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THCA (tumor)THCA (normal)
CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (tumor)CASR, UBC, PRKCG, PRKCA, VCP, FLNA, RNF19A, TMED2, PRKCB, CHD8, PI4K2B (normal)
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TissGeneProg for CASR

check button Kaplan-Meier plots with logrank tests of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image to enlarge it in a new window.
survival 1

check button Kaplan-Meier plots with logrank test of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 2

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 3

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 4

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TissGeneClin for CASR
TissGeneDrug for CASR

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status
DB01012CinacalcetAgonistSmall moleculeApproved


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TissGeneDisease for CASR

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0342637Hypocalciuric hypercalcemia, familial, type 1103BeFree,CLINVAR,CTD_human,GAD,MGD,ORPHANET,UNIPROT
umls:C0020437Hypercalcemia57BeFree,CTD_human,GAD,LHGDN
umls:C0342345Hypoparathyroidism - autosomal dominant40BeFree,CLINVAR
umls:C0221002Hyperparathyroidism, Primary25BeFree,GAD,LHGDN
umls:C0020502Hyperparathyroidism24BeFree,CTD_human,GAD,LHGDN
umls:C0020626Hypoparathyroidism23BeFree,CTD_human,GAD,LHGDN
umls:C0020438Hypercalciuria20BeFree,GAD,LHGDN,RGD
umls:C0699790Colon Carcinoma19BeFree
umls:C3715128HYPOCALCEMIA, AUTOSOMAL DOMINANT 117BeFree,MGD,ORPHANET,UNIPROT
umls:C0020503Hyperparathyroidism, Secondary16BeFree,GAD
umls:C1527249Colorectal Cancer16BeFree,GAD
umls:C0007102Malignant tumor of colon15BeFree
umls:C0009402Colorectal Carcinoma13BeFree
umls:C0262587Parathyroid Adenoma13BeFree
umls:C0006142Malignant neoplasm of breast12BeFree
umls:C0678222Breast Carcinoma12BeFree
umls:C0376358Malignant neoplasm of prostate10BeFree,GAD
umls:C0600139Prostate carcinoma10BeFree
umls:C0342342Idiopathic Hypoparathyroidism9BeFree
umls:C0596263Carcinogenesis9BeFree
umls:C0001430Adenoma8BeFree
umls:C0023418leukemia8BeFree
umls:C0149521Pancreatitis, Chronic8BeFree,GAD,LHGDN
umls:C0022650Kidney Calculi7BeFree,GAD
umls:C0029456Osteoporosis7BeFree
umls:C0392525Nephrolithiasis7BeFree
umls:C0002395Alzheimer's Disease6BeFree,GAD
umls:C0005684Malignant neoplasm of urinary bladder6BeFree,GAD
umls:C0178874Tumor Progression6BeFree
umls:C1561643Chronic Kidney Diseases6BeFree
umls:C0011860Diabetes Mellitus, Non-Insulin-Dependent5BeFree
umls:C0020598Hypocalcemia5CTD_human,GAD,LHGDN
umls:C0025517Metabolic Diseases5BeFree
umls:C0027627Neoplasm Metastasis5BeFree,LHGDN
umls:C0027819Neuroblastoma5BeFree
umls:C0030305Pancreatitis5BeFree,LHGDN
umls:C0030521Parathyroid Neoplasms5BeFree
umls:C0699885Carcinoma of bladder5BeFree
umls:C0700095Central neuroblastoma5BeFree
umls:C1832615HYPERPARATHYROIDISM, NEONATAL SEVERE5CLINVAR,CTD_human,MGD,ORPHANET,UNIPROT
umls:C2239176Liver carcinoma5BeFree
umls:C0004775Bartter Disease4BeFree
umls:C0009404Colorectal Neoplasms4BeFree,LHGDN
umls:C0011849Diabetes Mellitus4BeFree
umls:C0020599Hypocalciuria4BeFree
umls:C0022661Kidney Failure, Chronic4BeFree,GAD,LHGDN
umls:C0023434Chronic Lymphocytic Leukemia4BeFree
umls:C0028754Obesity4BeFree
umls:C0280100Solid tumour4BeFree
umls:C0345406Neonatal hyperparathyroidism4BeFree
umls:C0376545Hematologic Neoplasms4BeFree
umls:C0403447Chronic Kidney Insufficiency4BeFree,GAD
umls:C0543800Idiopathic hypercalciuria4BeFree
umls:C0687150Parathyroid Gland Adenocarcinoma4BeFree
umls:C0004153Atherosclerosis3BeFree,RGD
umls:C0020538Hypertensive disease3BeFree,GAD
umls:C0027051Myocardial Infarction3BeFree,LHGDN,RGD
umls:C0027709Nephrocalcinosis3BeFree
umls:C0029463Osteosarcoma3BeFree
umls:C0029925Ovarian Carcinoma3BeFree
umls:C0035078Kidney Failure3BeFree
umls:C0042870Vitamin D Deficiency3BeFree,LHGDN
umls:C0085859Polyglandular Type I Autoimmune Syndrome3BeFree
umls:C0149911Humoral hypercalcemia of malignancy (disorder)3BeFree
umls:C0238462Medullary carcinoma of thyroid3BeFree
umls:C0451641Urolithiasis3BeFree
umls:C0585442Osteosarcoma of bone3BeFree
umls:C1140680Malignant neoplasm of ovary3BeFree
umls:C1809471Familial benign hypercalcemia3BeFree,CLINVAR,ORPHANET
umls:C1833683NEPHROLITHIASIS, CALCIUM OXALATE3BeFree
umls:C1864729HYPERPARATHYROIDISM 33BeFree
umls:C0003850Arteriosclerosis2BeFree
umls:C0004114Astrocytoma2BeFree
umls:C0006705Calcium Metabolism Disorders2BeFree
umls:C0010054Coronary Arteriosclerosis2BeFree
umls:C0010068Coronary heart disease2BeFree
umls:C0014130Endocrine System Diseases2BeFree,GAD
umls:C0014544Epilepsy2BeFree
umls:C0017150Gastrinoma2BeFree
umls:C0017178Gastrointestinal Diseases2BeFree
umls:C0017638Glioma2BeFree
umls:C0019348Herpes Simplex Infections2BeFree
umls:C0020507Hyperplasia2LHGDN
umls:C0021670insulinoma2BeFree
umls:C0022658Kidney Diseases2BeFree,LHGDN
umls:C0023467Leukemia, Myelocytic, Acute2BeFree
umls:C0023903Liver neoplasms2BeFree
umls:C0024299Lymphoma2BeFree
umls:C0025202melanoma2BeFree
umls:C0026764Multiple Myeloma2BeFree
umls:C0030517Parathyroid Diseases2BeFree
umls:C0036572Seizures2BeFree
umls:C0085110Severe Combined Immunodeficiency2BeFree
umls:C0242379Malignant neoplasm of lung2BeFree,GAD
umls:C0271846Familial hyperparathyroidism2BeFree
umls:C0391957idiopathic epilepsy2BeFree
umls:C1261473Sarcoma2BeFree
umls:C1292769Precursor B-cell lymphoblastic leukemia2BeFree
umls:C1832648Hypoparathyroidism familial isolated2BeFree,CLINVAR,CTD_human
umls:C2316810Chronic kidney disease stage 52BeFree
umls:C0001925Albuminuria1RGD
umls:C0002063Alkalosis1BeFree
umls:C0002736Amyotrophic Lateral Sclerosis1BeFree
umls:C0003130Anoxia1RGD
umls:C0003507Aortic Valve Stenosis1GAD
umls:C0004364Autoimmune Diseases1BeFree
umls:C0006663Calcinosis1GAD
umls:C0007113Rectal Carcinoma1BeFree
umls:C0007134Renal Cell Carcinoma1BeFree
umls:C0007193Cardiomyopathy, Dilated1BeFree
umls:C0007222Cardiovascular Diseases1BeFree
umls:C0009319Colitis1BeFree
umls:C0009375Colonic Neoplasms1GAD,LHGDN
umls:C0011847Diabetes1BeFree
umls:C0011853Diabetes Mellitus, Experimental1RGD
umls:C0012242Digestive System Disorders1BeFree
umls:C0019034Hemoglobin SC Disease1BeFree
umls:C0020542Pulmonary Hypertension1RGD
umls:C0020676Hypothyroidism1BeFree
umls:C0021051Immunologic Deficiency Syndromes1BeFree
umls:C0021390Inflammatory Bowel Diseases1BeFree
umls:C0022680Polycystic Kidney Diseases1BeFree
umls:C0022951Lactose Intolerance1BeFree
umls:C0023530Leukopenia1BeFree
umls:C0023890Liver Cirrhosis1BeFree
umls:C0024117Chronic Obstructive Airway Disease1GAD
umls:C0025267Multiple Endocrine Neoplasia Type 11BeFree
umls:C0026269Mitral Valve Stenosis1GAD
umls:C0027055Myocardial Reperfusion Injury1RGD
umls:C0027947Neutropenia1BeFree
umls:C0032000Pituitary Adenoma1BeFree
umls:C0033578Prostatic Neoplasms1BeFree
umls:C0042769Virus Diseases1BeFree
umls:C0042963Vomiting1BeFree
umls:C0079731B-Cell Lymphomas1BeFree
umls:C0085207Gestational Diabetes1BeFree
umls:C0086543Cataract1BeFree
umls:C0149782Squamous cell carcinoma of lung1BeFree
umls:C0153381Malignant neoplasm of mouth1BeFree
umls:C0153676Secondary malignant neoplasm of lung1BeFree
umls:C0153690Secondary malignant neoplasm of bone1BeFree
umls:C0220641Lip and Oral Cavity Carcinoma1BeFree
umls:C0220989Acquired partial lipodystrophy1BeFree
umls:C0235974Pancreatic carcinoma1BeFree
umls:C0238461Anaplastic thyroid carcinoma1BeFree
umls:C0268450Gitelman Syndrome1BeFree
umls:C0268800Simple renal cyst1BeFree
umls:C0270850Idiopathic generalized epilepsy1BeFree,CTD_human
umls:C0282687Hemorrhagic Fever, Ebola1BeFree
umls:C0333186Restenosis1BeFree
umls:C0333983Hyperplastic Polyp1BeFree
umls:C0334634Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse1BeFree
umls:C0342634Neonatal hypocalcemia1BeFree
umls:C0342639Familial idiopathic hypercalciuria1BeFree
umls:C0346647Malignant neoplasm of pancreas1BeFree
umls:C0521707Bilateral cataracts (disorder)1BeFree
umls:C0549473Thyroid carcinoma1BeFree
umls:C0598935Tumor Initiation1BeFree
umls:C0684249Carcinoma of lung1BeFree
umls:C0745106hyperparathyroid1BeFree
umls:C0751956Acute Cerebrovascular Accidents1BeFree
umls:C0853897Diabetic Cardiomyopathies1RGD
umls:C0854110Insulin resistant diabetes1BeFree
umls:C0854467Myelosuppression1BeFree
umls:C0860204Cholestatic liver disease1BeFree
umls:C0878544Cardiomyopathies1RGD
umls:C1290807Diarrheal disorder1BeFree
umls:C1302401Adenoma of large intestine1BeFree
umls:C1458155Mammary Neoplasms1LHGDN
umls:C1519689Tumor Promotion1BeFree
umls:C1623038Cirrhosis1BeFree
umls:C1704436Peripheral Arterial Diseases1BeFree
umls:C1704981Hyperparathyroidism-Jaw Tumor Syndrome1BeFree
umls:C1833372HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III1BeFree
umls:C1835171Hypomagnesemia 2, renal1BeFree
umls:C1865868ALZHEIMER DISEASE 51BeFree
umls:C1956346Coronary Artery Disease1BeFree,LHGDN
umls:C2752062EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 81CLINVAR,UNIPROT
umls:C3163620Hypotension Adverse Event1GAD
umls:C3494489Autoimmune polyendocrinopathy syndrome, type 11BeFree
umls:C1832611Hypercalciuric Hypercalcemia0CLINVAR
umls:C1840402HYPERPARATHYROIDISM 10MGD