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| TissGeneSummary for CP |
 Gene summary |
| Basic gene information | Gene symbol | CP |
| Gene name | ceruloplasmin (ferroxidase) | |
| Synonyms | CP-2 | |
| Cytomap | UCSC genome browser: 3q23-q25 | |
| Type of gene | protein-coding | |
| RefGenes | NM_000096.3, NR_046371.1, | |
| Description | ceruloplasmin | |
| Modification date | 20141219 | |
| dbXrefs | MIM : 117700 | |
| HGNC : HGNC | ||
| Ensembl : ENSG00000047457 | ||
| HPRD : 00317 | ||
| Vega : OTTHUMG00000159563 | ||
| Protein | UniProt: go to UniProt's Cross Reference DB Table | |
| Expression | CleanEX: HS_CP | |
| BioGPS: 1356 | ||
| Pathway | NCI Pathway Interaction Database: CP | |
| KEGG: CP | ||
| REACTOME: CP | ||
| Pathway Commons: CP | ||
| Context | iHOP: CP | |
| ligand binding site mutation search in PubMed: CP | ||
| UCL Cancer Institute: CP | ||
| Assigned class in TissGDB* | C | |
| Included tissue-specific gene expression resources | HPA,GTEx | |
| Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx) | Liver | |
| Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA) | LIHC | |
| Reference showing the relevant tissue of CP | ||
| Description by TissGene annotations | Cancer gene | |
| * 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. |
| Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez |
| GO ID | GO term | PubMed ID |
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| TissGeneExp for CP |
| 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) |
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| 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) |
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| 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. |
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| 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) |
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| - Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05) |
| Cancer type | Mean(exp) in tumor | Mean(exp) in matched normal | Log2FC | P-val. | FDR |
| THCA | -2.249846135 | -0.217400373 | -2.032445763 | 1.17E-07 | 5.06E-07 |
| LUAD | 4.187165612 | 1.338744923 | 2.84842069 | 6.26E-12 | 4.49E-11 |
| COAD | -3.167923645 | 0.452214816 | -3.620138462 | 1.61E-11 | 2.99E-10 |
| KICH | -6.031259491 | -0.298367491 | -5.732892 | 4.00E-20 | 2.94E-18 |
| BRCA | 0.221173386 | 1.801754088 | -1.580580702 | 1.10E-05 | 2.71E-05 |
| LIHC | 6.813160509 | 8.698732509 | -1.885572 | 2.53E-08 | 2.02E-07 |
| KIRC | 4.67999612 | 0.265189175 | 4.414806944 | 9.39E-24 | 1.01E-22 |
| HNSC | -1.746611212 | 0.899984137 | -2.646595349 | 4.13E-05 | 0.000202893 |
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| TissGene-miRNA for CP |
| 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 type | miRNA id | miRNA accession | P-val. | Coeff. | # samples |
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| TissGeneMut for CP |
| TissGeneSNV for CP |
| 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. |
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| 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) |
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| - nsSNVs sorted by frequency. |
| AAchange | Cancer type | # samples |
| p.E251K | UCEC | 3 |
| p.E594K | SKCM | 2 |
| p.N340K | LIHC | 1 |
| p.E731D | UCEC | 1 |
| p.I861M | STAD | 1 |
| p.E208X | STAD | 1 |
| p.A133D | LUAD | 1 |
| p.E1027* | UCEC | 1 |
| p.E169G | LGG | 1 |
| p.N263S | HNSC | 1 |
| p.E925D | CHOL | 1 |
| p.D531G | STAD | 1 |
| p.E129K | SKCM | 1 |
| p.F920L | UCEC | 1 |
| p.F578L | UCEC | 1 |
| p.Q970H | GBM | 1 |
| p.T83S | LUAD | 1 |
| p.N956K | STAD | 1 |
| p.N384K | LIHC | 1 |
| p.E210* | UCEC | 1 |
| p.L805Q | GBM | 1 |
| p.H566N | UCS | 1 |
| p.G195R | COAD | 1 |
| p.G838R | LUAD | 1 |
| p.K148* | SARC | 1 |
| p.D611H | BLCA | 1 |
| p.S865F | BLCA | 1 |
| p.E216X | READ | 1 |
| p.G708D | GBM | 1 |
| p.D146Y | LUSC | 1 |
| p.S191L | CESC | 1 |
| p.E251K | COAD | 1 |
| p.V1056I | UCEC | 1 |
| p.S865F | STAD | 1 |
| p.L592F | SKCM | 1 |
| p.G569W | KIRP | 1 |
| p.R367H | COAD | 1 |
| p.Y260H | SKCM | 1 |
| p.S241L | BLCA | 1 |
| p.S622P | COAD | 1 |
| p.F351L | LUAD | 1 |
| p.K110I | UCEC | 1 |
| p.L666M | READ | 1 |
| p.G563R | SKCM | 1 |
| p.F92L | LGG | 1 |
| p.E954K | READ | 1 |
| p.H120Y | BLCA | 1 |
| p.R793H | DLBC | 1 |
| p.D703G | UCEC | 1 |
| p.N263D | LGG | 1 |
| p.N762T | BRCA | 1 |
| p.G418S | SKCM | 1 |
| p.I390M | LIHC | 1 |
| p.G708S | UCEC | 1 |
| p.L808I | UCEC | 1 |
| p.K42N | UCEC | 1 |
| p.W89C | LUAD | 1 |
| p.M557I | SKCM | 1 |
| p.K68N | BRCA | 1 |
| p.M965T | PAAD | 1 |
| p.W743* | SKCM | 1 |
| p.M158I | READ | 1 |
| p.D206N | LUAD | 1 |
| p.N716D | THYM | 1 |
| p.N365H | KIRP | 1 |
| p.G264E | SKCM | 1 |
| p.G988C | HNSC | 1 |
| p.S79P | BRCA | 1 |
| p.R258K | SKCM | 1 |
| p.P387S | SKCM | 1 |
| p.E380K | SKCM | 1 |
| p.F600V | PRAD | 1 |
| p.D184N | CESC | 1 |
| p.R436G | SARC | 1 |
| p.Y24H | PAAD | 1 |
| p.P477L | LUAD | 1 |
| p.R864K | SKCM | 1 |
| p.D252V | LIHC | 1 |
| p.S1002I | PRAD | 1 |
| p.E208* | STAD | 1 |
| p.Y155H | UCEC | 1 |
| p.T701I | LUAD | 1 |
| p.E943K | ESCA | 1 |
| p.D573Y | UCEC | 1 |
| p.E842D | UCS | 1 |
| p.E950D | ACC | 1 |
| p.G195R | STAD | 1 |
| p.N306K | GBM | 1 |
| p.V886G | ESCA | 1 |
| p.V643M | COAD | 1 |
| p.Q1058K | BRCA | 1 |
| p.R481S | COAD | 1 |
| p.S1012G | CHOL | 1 |
| p.D654N | STAD | 1 |
| p.E616G | LIHC | 1 |
| p.D595Y | COAD | 1 |
| p.Y260C | OV | 1 |
| p.E153* | LUAD | 1 |
| p.P876S | HNSC | 1 |
| p.R436Q | COAD | 1 |
| p.G771E | LUSC | 1 |
| p.F351L | COAD | 1 |
| p.A530S | READ | 1 |
| p.N483S | COAD | 1 |
| p.A737T | PRAD | 1 |
| p.G170R | SKCM | 1 |
| p.G132V | UCEC | 1 |
| p.G447C | LUAD | 1 |
| p.S492C | THYM | 1 |
| p.Y239* | LUAD | 1 |
| p.E216K | UCEC | 1 |
| p.D214N | LUAD | 1 |
| p.E723Q | HNSC | 1 |
| p.D279V | LUAD | 1 |
| p.I311V | BLCA | 1 |
| p.P582S | HNSC | 1 |
| p.Y67C | KIRP | 1 |
| p.G168A | SKCM | 1 |
| p.A161V | STAD | 1 |
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| TissGeneCNV for CP |
| 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) |
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| TissGeneFusions for CP |
| Fusion genes including TissGene (ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01) |
| Database | Src | Cancer type | Sample | Fusion gene | ORF | 5'-gene BP | 3'-gene BP |
| Chimerdb3.0 | ChiTaRs | NA | BG945303 | ATXN7-CP | chr3:63951571 | chr3:148911232 | |
| Chimerdb3.0 | FusionScan | BRCA | TCGA-BH-A18V-06A | CP-SOX5 | Out-of-Frame | chr3:148939433 | chr12:23999127 |
| TCGAfusionPortal | PRADA | BRCA | TCGA-AR-A0U4-01A | CP-WWTR1 | CDS-5UTR | Chr3:148905839 | Chr3:149387678 |
| TCGAfusionPortal | PRADA | BRCA | TCGA-BH-A18V-01A | CP-SOX5 | Out-of-frame | Chr3:148939434 | Chr12:23999127 |
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| TissGeneNet for CP |
| 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) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| COAD (tumor) | COAD (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| HNSC (tumor) | HNSC (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| KICH (tumor) | KICH (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| KIRC (tumor) | KIRC (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| KIRP (tumor) | KIRP (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| LIHC (tumor) | LIHC (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| LUAD (tumor) | LUAD (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| LUSC (tumor) | LUSC (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| PRAD (tumor) | PRAD (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| STAD (tumor) | STAD (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| THCA (tumor) | THCA (normal) |
| CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (tumor) | CP, UBC, HIF1A, BTRC, PITX3, PLG, RAD21, LTF, MPO, SLC40A1, PROC, ATP7A, GAST (normal) |
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| TissGeneProg for CP |
| 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. |
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| 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. |
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| 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. |
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| 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. |
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| TissGeneClin for CP |
| TissGeneDrug for CP |
| Drug information targeting TissGene (DrugBank Version 5.0.6, 2017-04-01) |
| DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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| TissGeneDisease for CP |
| Disease information associated with TissGene (DisGeNet, 2016-06-01) |
| Disease ID | Disease name | # pubmeds | Source |
| umls:C0878682 | Ceruloplasmin deficiency | 28 | BeFree,CLINVAR,MGD,ORPHANET |
| umls:C0019202 | Hepatolenticular Degeneration | 26 | BeFree,CTD_human |
| umls:C0282193 | Iron Overload | 12 | BeFree,CTD_human |
| umls:C0012715 | Iron Metabolism Disorders | 8 | BeFree,CTD_human,RGD |
| umls:C0152457 | Kayser-Fleischer ring | 8 | BeFree |
| umls:C0524851 | Neurodegenerative Disorders | 8 | BeFree |
| umls:C0030567 | Parkinson Disease | 7 | BeFree,CTD_human,GAD,LHGDN |
| umls:C0002395 | Alzheimer's Disease | 6 | BeFree,GAD,LHGDN |
| umls:C0011849 | Diabetes Mellitus | 6 | BeFree,CTD_human,LHGDN |
| umls:C0018995 | Hemochromatosis | 5 | BeFree,CTD_human,LHGDN |
| umls:C0235031 | Neurologic Symptoms | 5 | BeFree |
| umls:C0268070 | Hypocupremia | 5 | BeFree |
| umls:C0002871 | Anemia | 4 | BeFree |
| umls:C0022716 | Menkes Kinky Hair Syndrome | 4 | BeFree,CTD_human |
| umls:C0023895 | Liver diseases | 4 | BeFree,LHGDN |
| umls:C0002878 | Anemia, Hemolytic | 3 | BeFree |
| umls:C0003873 | Rheumatoid Arthritis | 3 | BeFree,CTD_human,LHGDN |
| umls:C0007222 | Cardiovascular Diseases | 3 | BeFree,LHGDN |
| umls:C0011854 | Diabetes Mellitus, Insulin-Dependent | 3 | BeFree,CTD_human,GAD |
| umls:C0017638 | Glioma | 3 | BeFree,LHGDN |
| umls:C0022116 | Ischemia | 3 | BeFree,CTD_human |
| umls:C0035304 | Retinal Degeneration | 3 | BeFree,CTD_human |
| umls:C0242383 | Age related macular degeneration | 3 | BeFree |
| umls:C2931082 | Familial apoceruloplasmin deficiency | 3 | CTD_human,ORPHANET |
| umls:C0002736 | Amyotrophic Lateral Sclerosis | 2 | GAD,LHGDN |
| umls:C0004352 | Autistic Disorder | 2 | BeFree,CTD_human |
| umls:C0009375 | Colonic Neoplasms | 2 | CTD_human,LHGDN |
| umls:C0011847 | Diabetes | 2 | BeFree |
| umls:C0013362 | Dysarthria | 2 | BeFree |
| umls:C0015230 | Exanthema | 2 | BeFree |
| umls:C0017601 | Glaucoma | 2 | BeFree |
| umls:C0017661 | IGA Glomerulonephritis | 2 | BeFree,CTD_human |
| umls:C0019114 | Hemosiderosis | 2 | BeFree |
| umls:C0027765 | nervous system disorder | 2 | BeFree |
| umls:C0040822 | Tremor | 2 | BeFree,LHGDN |
| umls:C0220756 | Niemann-Pick Disease, Type C | 2 | BeFree |
| umls:C0238339 | Hereditary pancreatitis | 2 | BeFree |
| umls:C0392514 | Hereditary hemochromatosis | 2 | BeFree |
| umls:C0848332 | Spots on skin | 2 | BeFree |
| umls:C0993582 | Arthritis, Experimental | 2 | CTD_human,RGD |
| umls:C2239176 | Liver carcinoma | 2 | BeFree,CTD_human |
| umls:C0000786 | Spontaneous abortion | 1 | GAD |
| umls:C0001925 | Albuminuria | 1 | CTD_human |
| umls:C0002875 | Cooley's anemia | 1 | BeFree |
| umls:C0002965 | Angina, Unstable | 1 | LHGDN |
| umls:C0003130 | Anoxia | 1 | GAD |
| umls:C0003850 | Arteriosclerosis | 1 | BeFree |
| umls:C0004134 | Ataxia | 1 | CTD_human |
| umls:C0004153 | Atherosclerosis | 1 | BeFree |
| umls:C0005747 | Blepharospasm | 1 | BeFree |
| umls:C0006111 | Brain Diseases | 1 | CTD_human |
| umls:C0007137 | Squamous cell carcinoma | 1 | BeFree |
| umls:C0007758 | Cerebellar Ataxia | 1 | BeFree |
| umls:C0007786 | Brain Ischemia | 1 | RGD |
| umls:C0011570 | Mental Depression | 1 | GAD |
| umls:C0011853 | Diabetes Mellitus, Experimental | 1 | RGD |
| umls:C0013080 | Down Syndrome | 1 | BeFree |
| umls:C0013384 | Dyskinetic syndrome | 1 | CTD_human |
| umls:C0013421 | Dystonia | 1 | LHGDN |
| umls:C0014544 | Epilepsy | 1 | BeFree |
| umls:C0015371 | Extrapyramidal Disorders | 1 | BeFree |
| umls:C0018799 | Heart Diseases | 1 | RGD |
| umls:C0018801 | Heart failure | 1 | BeFree |
| umls:C0018802 | Congestive heart failure | 1 | BeFree |
| umls:C0019188 | Hepatitis, Animal | 1 | RGD |
| umls:C0019189 | Hepatitis, Chronic | 1 | CTD_human |
| umls:C0020179 | Huntington Disease | 1 | LHGDN |
| umls:C0020550 | Hyperthyroidism | 1 | RGD |
| umls:C0022658 | Kidney Diseases | 1 | BeFree |
| umls:C0023904 | Liver Neoplasms, Experimental | 1 | CTD_human |
| umls:C0024437 | Macular degeneration | 1 | BeFree |
| umls:C0025202 | melanoma | 1 | CTD_human |
| umls:C0026650 | Movement Disorders | 1 | BeFree |
| umls:C0027051 | Myocardial Infarction | 1 | BeFree |
| umls:C0027746 | Nerve Degeneration | 1 | CTD_human |
| umls:C0028754 | Obesity | 1 | BeFree |
| umls:C0029925 | Ovarian Carcinoma | 1 | BeFree |
| umls:C0032914 | Pre-Eclampsia | 1 | CTD_human,LHGDN |
| umls:C0033860 | Psoriasis | 1 | CTD_human |
| umls:C0034150 | Purpura | 1 | LHGDN |
| umls:C0035334 | Retinitis Pigmentosa | 1 | BeFree |
| umls:C0036341 | Schizophrenia | 1 | CTD_human |
| umls:C0036572 | Seizures | 1 | BeFree |
| umls:C0040034 | Thrombocytopenia | 1 | LHGDN |
| umls:C0040136 | Thyroid Neoplasm | 1 | RGD |
| umls:C0042384 | Vasculitis | 1 | BeFree |
| umls:C0085397 | Pasteurellaceae Infections | 1 | CTD_human |
| umls:C0151731 | Hepatic infarction | 1 | BeFree |
| umls:C0232197 | Fibrillation | 1 | BeFree |
| umls:C0235974 | Pancreatic carcinoma | 1 | BeFree |
| umls:C0240066 | Iron deficiency | 1 | BeFree |
| umls:C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | 1 | BeFree |
| umls:C0341439 | Chronic liver disease | 1 | BeFree |
| umls:C0346647 | Malignant neoplasm of pancreas | 1 | BeFree |
| umls:C0374997 | Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site | 1 | BeFree |
| umls:C0400966 | Non-alcoholic Fatty Liver Disease | 1 | BeFree |
| umls:C0403440 | Thin basement membrane disease | 1 | BeFree |
| umls:C0426980 | Motor symptoms | 1 | BeFree |
| umls:C0497327 | Dementia | 1 | CTD_human |
| umls:C0524620 | Metabolic Syndrome X | 1 | BeFree |
| umls:C0740457 | Malignant neoplasm of kidney | 1 | BeFree |
| umls:C0741923 | cardiac event | 1 | BeFree |
| umls:C0854279 | Basal ganglion degeneration | 1 | BeFree |
| umls:C0919267 | ovarian neoplasm | 1 | BeFree |
| umls:C0948089 | Acute Coronary Syndrome | 1 | BeFree |
| umls:C1140680 | Malignant neoplasm of ovary | 1 | BeFree |
| umls:C1266042 | Chromophobe Renal Cell Carcinoma | 1 | BeFree |
| umls:C1306837 | Papillary Renal Cell Carcinoma | 1 | BeFree |
| umls:C1527311 | Brain Edema | 1 | RGD |
| umls:C1833213 | Hyperferritinemia, hereditary, with congenital cataracts | 1 | BeFree |
| umls:C2930898 | Benign essential blepharospasm | 1 | BeFree |
| umls:C2931845 | Neurodegeneration with brain iron accumulation (NBIA) | 1 | BeFree |
| umls:C3714619 | Insulin resistance syndrome | 1 | BeFree |
| umls:C1858583 | HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA | 0 | CLINVAR |
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