| No. |
Resource ID |
Entrez DB |
Entrez OID |
Link Name |
Link Category |
Link Url |
Link Query |
| 1
|
nlx_31015
|
PubMed
|
14530391
|
This paper describes that Genetic obesity is related to multiple genes--CARTPT, FFAR4, SLC6A14, SDC3, POMC, GHRL, SIM1, ADRB2, UCP3, PCSK1, FTO, NR0B2, PPARG, MC4R, UCP2, MC3R, AQP7, MRAP2, ADCY3, PPARGC1B, ENPP1, ADRB3, AGRP, UCP1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 2
|
nlx_31015
|
PubMed
|
25329695
|
This paper describes that Isolated anhidrosis with normal sweat glands, Dann-Epstein-Sohar syndrome is related to a gene--ITPR2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 3
|
nlx_31015
|
PubMed
|
15103726
|
This paper describes that Ablepharon-macrostomia syndrome is related to a gene--TWIST2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 4
|
nlx_31015
|
PubMed
|
24269013
|
This paper describes that Rasmussen encephalitis, Rasmussen syndrome is related to multiple genes--PDCD1, CTLA4--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 5
|
nlx_31015
|
PubMed
|
11175791
|
This paper describes that Nail-patella syndrome is related to a gene--LMX1B--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 6
|
nlx_31015
|
PubMed
|
18567738
|
This paper describes that Defects in the degradation of sphingomyelin is related to multiple genes--ASAH1, SMPD1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 7
|
nlx_31015
|
PubMed
|
21695231
|
This paper describes that Myopia is related to multiple genes--ZNF644, ARR3, P3H2, SCO2, PRIMPOL, LRPAP1, SLC39A5, P4HA2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 8
|
nlx_31015
|
PubMed
|
11978965
|
This paper describes that Williams-Beuren syndrome is related to multiple genes--ELN, GTF2I, EIF4H, MLXIPL, SPDYE1, TMEM270, LAT2, FZD9, STX1A, BUD23, RCC1L, METTL27, LIMK1, CLIP2, RFC2, CLDN4, DNAJC30, ABHD11, TRIM50, GALNT17, BCL7B, GTF2IRD1, TBL2, FKBP6, BAZ1B, CLDN3, NSUN5, VPS37D--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 9
|
nlx_31015
|
PubMed
|
17647025
|
This paper describes that Hypertension exacerbated in pregnancy is related to a gene--NR3C2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 10
|
nlx_31015
|
PubMed
|
2191710
|
This paper describes that KID/HID syndrome is related to a gene--GJB2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 11
|
nlx_31015
|
PubMed
|
17525176
|
This paper describes that Aland Island eye disease, Forsius-Eriksson syndrome is related to a gene--CACNA1F--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 12
|
nlx_31015
|
PubMed
|
20301770
|
This paper describes that Feingold syndrome is related to multiple genes--MYCN, MIR17HG--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 13
|
nlx_31015
|
PubMed
|
8189372
|
This paper describes that Laryngeal cancer is related to multiple genes--TP53, CCND1, EGFR, CDKN2A, MYC, CCNE1, CCNE2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 14
|
nlx_31015
|
PubMed
|
20838246
|
This paper describes that Leukoencephalopathy with vanishing white matter, Vanishing white matter disease, Childhood ataxia with diffuse central nervous system hypomyelination (CACH), Cree leukoencephalopathy (CLE) is related to multiple genes--EIF2B1, EIF2B2, EIF2B5, EIF2B4, EIF2B3--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 15
|
nlx_31015
|
PubMed
|
26206677
|
This paper describes that Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation is related to a gene--PLCG2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 16
|
nlx_31015
|
PubMed
|
17870445
|
This paper describes that Odontoonychodermal dysplasia is related to a gene--WNT10A--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 17
|
nlx_31015
|
PubMed
|
20159981
|
This paper describes that Cataract is related to multiple genes--HSF4, BFSP2, FYCO1, LIM2, BFSP1, WFS1, CRYGD, CRYBB1, CRYBA4, LEMD2, GJA8, EPHA2, CRYAA, PITX3, GCNT2, CRYGS, FOXE3, TDRD7, SIPA1L3, CRYGC, CRYBB2, CRYBA1, GJA3, MIP, CRYAB, MAF, CRYBB3, VIM, CHMP4B, AGK, CRYGB, NHS, CRYBA2, UNC45B, LSS, SLC16A12--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 18
|
nlx_31015
|
PubMed
|
26284562
|
This paper describes that Ulcerative colitis is related to multiple genes--IL23R, IL10, MST1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 19
|
nlx_31015
|
PubMed
|
20460441
|
This paper describes that Scapuloperoneal spinal muscular atrophy is related to a gene--TRPV4--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 20
|
nlx_31015
|
PubMed
|
20507343
|
This paper describes that Woodhouse-Sakati syndrome, Hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome is related to a gene--DCAF17--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 21
|
nlx_31015
|
PubMed
|
27061120
|
This paper describes that Primrose syndrome is related to a gene--ZBTB20--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 22
|
nlx_31015
|
PubMed
|
19438883
|
This paper describes that Hereditary mixed polyposis syndrome is related to a gene--BMPR1A--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 23
|
nlx_31015
|
PubMed
|
21463272
|
This paper describes that Dravet syndrome is related to a gene--SCN1A--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 24
|
nlx_31015
|
PubMed
|
25480035
|
This paper describes that Autosomal recessive mental retardation is related to multiple genes--GRIK2, TECR, HERC2, TAF2, PIGG, PUS3, PRSS12, CRBN, TRAPPC9, MED23, ANK3, TTI2, WASHC4, FBXO31, FMN2, GPT2, EDC3, LMAN2L, TNIK, ZC3H14, IMPA1, ST3GAL3, MAN1B1, LINS1, ADAT3, KPTN, PGAP1, METTL23, NDST1, HNMT, ELP2, CC2D1A, NSUN2, TUSC3, CRADD, SLC6A17, MBOAT7, TAF13--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 25
|
nlx_31015
|
PubMed
|
11484200
|
This paper describes that 3C syndrome, Ritscher-Schinzel syndrome, Craniocerebellocardiac dysplasia is related to multiple genes--WASHC5, CCDC22--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 26
|
nlx_31015
|
PubMed
|
17498019
|
This paper describes that Long QT syndrome is related to multiple genes--KCNQ1, ANK2, CAV3, KCNJ5, CALM2, SCN5A, CACNA1C, AKAP9, SNTA1, KCNE1, KCNJ2, SCN4B, KCNH2, KCNE2, CALM1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 27
|
nlx_31015
|
PubMed
|
20301453
|
This paper describes that Tetra-amelia is related to a gene--WNT3--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 28
|
nlx_31015
|
PubMed
|
11477132
|
This paper describes that Colorectal cancer is related to multiple genes--SMAD2, TP53, MSH6, EREG, CTNNB1, KRAS, TGFBR2, BAX, MLH1, MSH2, GALNT12, AREG, DCC, MSH3, TGFA, APC2, SMAD4, EGF--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 29
|
nlx_31015
|
PubMed
|
17803606
|
This paper describes that Pseudofolliculitis barbae is related to a gene--KRT75--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 30
|
nlx_31015
|
PubMed
|
17499497
|
This paper describes that Parkinson disease is related to multiple genes--SNCA, PARK7, GIGYF2, EIF4G1, PRKN, PLA2G6, CHCHD2, PINK1, LRRK2, HTRA2, FBXO7, VPS35, UCHL1, ATP13A2, DNAJC16, NR4A2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 31
|
nlx_31015
|
PubMed
|
21464306
|
This paper describes that Perrault syndrome is related to multiple genes--HARS2, TWNK, HSD17B4, LARS2, CLPP, ERAL1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 32
|
nlx_31015
|
PubMed
|
18325042
|
This paper describes that Focal dermal hypoplasia, Goltz-Gorlin syndrome is related to a gene--PORCN--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 33
|
nlx_31015
|
PubMed
|
21763481
|
This paper describes that Meckel syndrome, Meckel-Gruber syndrome is related to multiple genes--MKS1, TMEM67, NPHP3, TCTN2, KIF14, CEP290, RPGRIP1L, TMEM107, TMEM216, CC2D2A, B9D1, B9D2, TMEM231--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 34
|
nlx_31015
|
PubMed
|
12196741
|
This paper describes that Ichthyosis hystrix, Curth-Macklin type is related to a gene--KRT1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 35
|
nlx_31015
|
PubMed
|
27426733
|
This paper describes that Frontometaphyseal dysplasia is related to multiple genes--MAP3K7, FLNA--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 36
|
nlx_31015
|
PubMed
|
12358886
|
This paper describes that Multiple myeloma is related to multiple genes--CCND1, FGFR3, TP53, NSD2, KRAS, NRAS, MYC, CCND3, MAF--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 37
|
nlx_31015
|
PubMed
|
25033069
|
This paper describes that Boucher-Neuhauser syndrome is related to a gene--PNPLA6--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 38
|
nlx_31015
|
PubMed
|
27461267
|
This paper describes that Juvenile idiopathic arthritis is related to multiple genes--IL6, MIF--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 39
|
nlx_31015
|
PubMed
|
16854371
|
This paper describes that Metachromatic leukodystrophy is related to multiple genes--ARSA, PSAP--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 40
|
nlx_31015
|
PubMed
|
15695383
|
This paper describes that Li-Fraumeni syndrome is related to multiple genes--TP53, CHEK2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 41
|
nlx_31015
|
PubMed
|
20648714
|
This paper describes that Glycogen storage disease type III, Cori disease, Forbes disease is related to a gene--AGL--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 42
|
nlx_31015
|
PubMed
|
9771708
|
This paper describes that SEMD, Pakistani type, Brachyolmia type 4 is related to a gene--PAPSS2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 43
|
nlx_31015
|
PubMed
|
12395297
|
This paper describes that Duane-radial ray syndrome, Okihiro syndrome is related to a gene--SALL4--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 44
|
nlx_31015
|
PubMed
|
25741866
|
This paper describes that Myopia is related to multiple genes--ZNF644, ARR3, P3H2, SCO2, PRIMPOL, LRPAP1, SLC39A5, P4HA2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 45
|
nlx_31015
|
PubMed
|
20835237
|
This paper describes that Senior-Loken syndrome is related to multiple genes--SDCCAG8, WDR19, NPHP4, CEP290, TRAF3IP1, NPHP1, IQCB1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 46
|
nlx_31015
|
PubMed
|
18157819
|
This paper describes that Sphingolipidosis is related to multiple genes--GLB1, ARSA, GLA, ASAH1, GBA, GALC, SMPD1, PSAP, SUMF1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 47
|
nlx_31015
|
PubMed
|
20507384
|
This paper describes that Epidermolysis bullosa, hemidesmosomal is related to a gene--PLEC--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 48
|
nlx_31015
|
PubMed
|
12621137
|
This paper describes that Colorectal cancer is related to multiple genes--SMAD2, TP53, MSH6, EREG, CTNNB1, KRAS, TGFBR2, BAX, MLH1, MSH2, GALNT12, AREG, DCC, MSH3, TGFA, APC2, SMAD4, EGF--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 49
|
nlx_31015
|
PubMed
|
19026859
|
This paper describes that Short QT syndrome is related to multiple genes--KCNQ1, KCNJ2, KCNH2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 50
|
nlx_31015
|
PubMed
|
21397062
|
This paper describes that Hypomagnesemia is related to multiple genes--TRPM6, CNNM2, CLDN16, CLDN19, FXYD2, EGF--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 51
|
nlx_31015
|
PubMed
|
15932923
|
This paper describes that SERKAL syndrome is related to a gene--WNT4--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 52
|
nlx_31015
|
PubMed
|
21282187
|
This paper describes that Beckwith-Wiedemann syndrome is related to multiple genes--KCNQ1OT1, CDKN1C, H19, NSD1, IGF2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 53
|
nlx_31015
|
PubMed
|
22510444
|
This paper describes that Bardet-Biedl syndrome is related to multiple genes--BBS1, BBS5, BBS9, MKS1, SDCCAG8, IFT27, MKKS, BBS7, BBS10, CEP290, IFT74, C8orf37, BBS2, ARL6, WDPCP, LZTFL1, BBS4, TTC8, TRIM32, BBS12, BBIP1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 54
|
nlx_31015
|
PubMed
|
9452994
|
This paper describes that X-linked hypercalciuric nephrolithiasis is related to a gene--CLCN5--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 55
|
nlx_31015
|
PubMed
|
10802654
|
This paper describes that Char syndrome is related to a gene--TFAP2B--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 56
|
nlx_31015
|
PubMed
|
1404302
|
This paper describes that Revesz syndrome, Exudative retinopathy with bone marrow failure is related to a gene--TINF2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 57
|
nlx_31015
|
PubMed
|
20013129
|
This paper describes that Schimke immunoosseous dysplasia is related to a gene--SMARCAL1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 58
|
nlx_31015
|
PubMed
|
10889272
|
This paper describes that Retinitis pigmentosa is related to multiple genes--RP9, CA4, EYS, NRL, FAM161A, MERTK, KLHL7, PDE6A, IMPG2, DHDDS, MAK, RBP3, PRPF4, AGBL5, RP2, RHO, ROM1, IMPDH1, CRB1, TULP1, PRPF3, RPE65, CERKL, FSCN2, PRCD, USH2A, PDE6B, PROM1, CNGA1, BEST1, PCARE, PRPF6, CLRN1, NEK2, SLC7A14, KIZ, IFT172, ZNF408, RP1, RPGR, PRPF31, ABCA4, OFD1, SEMA4A, NR2E3, RGR, IDH3B, SAG, ARL6, ZNF513, BBS2, ARL2BP, PRPH2, PRPF8, TOPORS, SNRNP200, CNGB1, GUCA1B, PDE6G, HGSNAT, RLBP1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 59
|
nlx_31015
|
PubMed
|
3099574
|
This paper describes that Fraser syndrome is related to multiple genes--FRAS1, GRIP1, FREM2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 60
|
nlx_31015
|
PubMed
|
19944693
|
This paper describes that Defects in the degradation of sphingomyelin is related to multiple genes--ASAH1, SMPD1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 61
|
nlx_31015
|
PubMed
|
18684024
|
This paper describes that Primary hyperparathyroidism, Familial hyperparathyroidism is related to multiple genes--MEN1, GCM2, CDC73, CASR--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 62
|
nlx_31015
|
PubMed
|
22017263
|
This paper describes that Choroideremia, Tapetochoroidal dystrophy is related to a gene--CHM--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 63
|
nlx_31015
|
PubMed
|
26482257
|
This paper describes that Combined immunodeficiency is related to multiple genes--IL2RG, RAG1, RFX5, ZAP70, CD8A, CD40LG, CD40, TAP1, ORAI1, LCK, IKBKB, TNFRSF4, CD3G, RAG2, CIITA, STIM1, CARD11, MALT1, CTPS1, BCL10, PNP, TAP2, RFXAP, RFXANK, DOCK2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 64
|
nlx_31015
|
PubMed
|
16441263
|
This paper describes that OFC syndrome, Oto-facio-cervical syndrome is related to multiple genes--EYA1, PAX1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 65
|
nlx_31015
|
PubMed
|
28777931
|
This paper describes that Combined oxidative phosphorylation deficiency is related to multiple genes--MRPS22, MRPL44, LYRM4, GTPBP3, NARS2, MARS2, CARS2, TRMT10C, C1QBP, MRPS16, TSFM, AARS2, EARS2, FARS2, SFXN4, VARS2, SLC25A26, MRPS34, GFM1, AIFM1, RMND1, ELAC2, TRMT5, MIPEP, TUFM, C12orf65, MRPL3, MTO1, PNPT1, MTFMT, TARS2, ATP5F1A, TXN2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 66
|
nlx_31015
|
PubMed
|
15161861
|
This paper describes that Adult i phenotype is related to a gene--GCNT2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 67
|
nlx_31015
|
PubMed
|
21497427
|
This paper describes that Hemophilia is related to multiple genes--F8, F9, VWF, GP1BA--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 68
|
nlx_31015
|
PubMed
|
18473821
|
This paper describes that Spinal and bulbar muscular atrophy (SBMA), Kennedy disease is related to a gene--AR--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 69
|
nlx_31015
|
PubMed
|
20634695
|
This paper describes that Andersen-Tawil syndrome is related to a gene--KCNJ2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 70
|
nlx_31015
|
PubMed
|
20064629
|
This paper describes that Peroxisomal beta-oxidation enzyme deficiency is related to multiple genes--SCP2, HSD17B4, ACOX1, AMACR--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 71
|
nlx_31015
|
PubMed
|
16368216
|
This paper describes that Glutaric acidemia is related to multiple genes--ETFB, GCDH, SUGCT, ETFA, ETFDH--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 72
|
nlx_31015
|
PubMed
|
28406212
|
This paper describes that Trehalase deficiency is related to a gene--TREH--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 73
|
nlx_31015
|
PubMed
|
18978332
|
This paper describes that Malignant paraganglioma is related to multiple genes--NF1, EPAS1, MAX, RET, TMEM127, SDHD, SDHB, SDHC, VHL, FH--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 74
|
nlx_31015
|
PubMed
|
15489140
|
This paper describes that Hepatocellular carcinoma, Liver cancer is related to multiple genes--TP53, FZD7, AXIN1, NFE2L2, TERT, PTEN, TGFBR2, CTNNB1, ARID2, TGFA, IGF2, IGF1R, MYC, CDKN2A, KEAP1, HGF, RB1, MET, PIK3CA, ARID1A--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 75
|
nlx_31015
|
PubMed
|
20413652
|
This paper describes that Congenital asplenia is related to multiple genes--RPSA, GDF1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 76
|
nlx_31015
|
PubMed
|
26111154
|
This paper describes that Lamb-Shaffer syndrome, 12p12.1 microdeletion syndrome is related to a gene--SOX5--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 77
|
nlx_31015
|
PubMed
|
21217752
|
This paper describes that Spondyloenchondrodysplasia with immune dysregulation (SPENCDI), Spondyloenchondrodysplasia (SPENCD) is related to a gene--ACP5--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 78
|
nlx_31015
|
PubMed
|
11145114
|
This paper describes that Hypermethioninemia is related to multiple genes--AHCY, ADK, MAT1A, GNMT--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 79
|
nlx_31015
|
PubMed
|
18646567
|
This paper describes that Nonaka distal myopathy (NM), Distal myopathy with rimmed vacuoles (DMRV), Hereditary inclusion body myopathy (hIBM) is related to a gene--GNE--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 80
|
nlx_31015
|
PubMed
|
25480037
|
This paper describes that Catel-Manzke syndrome, Palatodigital syndrome, Hyperphalangy syndrome is related to a gene--TGDS--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 81
|
nlx_31015
|
PubMed
|
6660246
|
This paper describes that 3MC syndrome, Malpuech-Michels-Mingarelli-Carnevale syndrome is related to multiple genes--COLEC10, MASP1, COLEC11--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 82
|
nlx_31015
|
PubMed
|
11181649
|
This paper describes that 3-Methylcrotonylglycinuria, 3-Methylcrotonyl-CoA carboxylase deficiency is related to multiple genes--MCCC1, MCCC2--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 83
|
nlx_31015
|
PubMed
|
18823727
|
This paper describes that Partington syndrome is related to a gene--ARX--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 84
|
nlx_31015
|
PubMed
|
21976959
|
This paper describes that Keratoconus is related to a gene--VSX1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 85
|
nlx_31015
|
PubMed
|
1867263
|
This paper describes that Metaphyseal dysplasias is related to multiple genes--COL10A1, SBDS, PTH1R, MMP9, RMRP, MMP13--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 86
|
nlx_31015
|
PubMed
|
8889589
|
This paper describes that Glycogen storage disease type VII, Tarui disease is related to a gene--PFKM--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 87
|
nlx_31015
|
PubMed
|
14999526
|
This paper describes that Osteoporosis is related to multiple genes--CALCR, COL1A1, TGFB1, MIR2861, COL1A2, LRP5, VDR, UGT2B17, LGR4, PLS3, PDLIM4, PTH, WNT1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 88
|
nlx_31015
|
PubMed
|
22265017
|
This paper describes that Genitopatellar syndrome is related to a gene--KAT6B--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 89
|
nlx_31015
|
PubMed
|
15070562
|
This paper describes that Bladder cancer is related to multiple genes--HRAS, FGFR3, TP53, DAPK1, EGFR, RASSF1, CDKN2A, ERBB2, RB1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 90
|
nlx_31015
|
PubMed
|
15805157
|
This paper describes that Acromesomelic dysplasia, Demirhan type, Acromesomelic dysplasia with genital anomalies is related to a gene--BMPR1B--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 91
|
nlx_31015
|
PubMed
|
22815638
|
This paper describes that Optic atrophy is related to multiple genes--YME1L1, DNM1L, TMEM126A, OPA1, OPA3, ACO2, RTN4IP1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 92
|
nlx_31015
|
PubMed
|
25968935
|
This paper describes that West syndrome, Infantile spasms is related to multiple genes--CDKL5, ST3GAL3, ARX--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 93
|
nlx_31015
|
PubMed
|
23401415
|
This paper describes that Williams-Beuren syndrome is related to multiple genes--ELN, GTF2I, EIF4H, MLXIPL, SPDYE1, TMEM270, LAT2, FZD9, STX1A, BUD23, RCC1L, METTL27, LIMK1, CLIP2, RFC2, CLDN4, DNAJC30, ABHD11, TRIM50, GALNT17, BCL7B, GTF2IRD1, TBL2, FKBP6, BAZ1B, CLDN3, NSUN5, VPS37D--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 94
|
nlx_31015
|
PubMed
|
22829454
|
This paper describes that Craniosynostoses is related to multiple genes--TCF12, MSX2, ALX4, ZIC1, TWIST1, ERF--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 95
|
nlx_31015
|
PubMed
|
17632693
|
This paper describes that Defects in the degradation of sphingomyelin is related to multiple genes--ASAH1, SMPD1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 96
|
nlx_31015
|
PubMed
|
9612070
|
This paper describes that Hypermethioninemia is related to multiple genes--AHCY, ADK, MAT1A, GNMT--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 97
|
nlx_31015
|
PubMed
|
21358632
|
This paper describes that Meier-Gorlin syndrome, Ear-patella-short statute syndrome is related to multiple genes--ORC4, ORC1, ORC6, CDT1, CDC6, GMNN, CDC45--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 98
|
nlx_31015
|
PubMed
|
10746614
|
This paper describes that Idiopathic hyperCKemia, Elevated serum creatine phosphokinase is related to a gene--CAV3--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 99
|
nlx_31015
|
PubMed
|
16652336
|
This paper describes that Epithelial basement membrane corneal dystrophy, Cogan microcystic epithelial dystrophy, Map-dot-fingerprint dystrophy is related to a gene--TGFBI--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
| 100
|
nlx_31015
|
PubMed
|
27490115
|
This paper describes that 46,XX testicular disorder of sex development is related to multiple genes--SRY, SOX3, NR5A1--noted by KEGG.
|
Data: Disease Annotation
|
Link
|
|
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