DISCO:  Extensible Web resource DISCOvery, registration and interoperation framework
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Links from: Clinical Genomic Database
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Imported: 2019-10-27 17:00:05.706      NCBI transfered: 2019-09-27 17:01:04.0
No. Resource ID Entrez DB Entrez OID Link Name Link Category Link Url Link Query
1 nlx_152872 PubMed 22665976 A relationship between CRYBA1 and the N/AADcataract 10, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
2 nlx_152872 PubMed 23508780 A relationship between CRYBA2 and the N/AADcataract 42 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
3 nlx_152872 PubMed 16960806 A relationship between CRYBA4 and the N/AADcataract 23 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
4 nlx_152872 PubMed 20577656 A relationship between CRYBA4 and the N/AADcataract 23 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
5 nlx_152872 PubMed 12360425 A relationship between CRYBB1 and the N/AAD/ARcataract 17, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
6 nlx_152872 PubMed 17460281 A relationship between CRYBB1 and the N/AAD/ARcataract 17, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
7 nlx_152872 PubMed 21972112 A relationship between CRYBB1 and the N/AAD/ARcataract 17, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
8 nlx_152872 PubMed 2240043 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
9 nlx_152872 PubMed 8812489 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
10 nlx_152872 PubMed 9158139 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
11 nlx_152872 PubMed 10634616 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
12 nlx_152872 PubMed 11424921 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
13 nlx_152872 PubMed 17234267 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
14 nlx_152872 PubMed 18617901 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
15 nlx_152872 PubMed 19649175 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
16 nlx_152872 PubMed 21031021 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
17 nlx_152872 PubMed 21245961 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
18 nlx_152872 PubMed 22312185 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
19 nlx_152872 PubMed 22846113 A relationship between CRYBB2 and the N/AADcataract 3, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
20 nlx_152872 PubMed 8190472 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
21 nlx_152872 PubMed 10521291 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
22 nlx_152872 PubMed 10914683 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
23 nlx_152872 PubMed 12011157 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
24 nlx_152872 PubMed 18587492 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
25 nlx_152872 PubMed 18618005 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
26 nlx_152872 PubMed 19204787 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
27 nlx_152872 PubMed 22052681 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
28 nlx_152872 PubMed 22876111 A relationship between CRYGC and the N/AADcataract 2, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
29 nlx_152872 PubMed 8733140 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
30 nlx_152872 PubMed 10521291 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
31 nlx_152872 PubMed 9927684 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
32 nlx_152872 PubMed 10915766 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
33 nlx_152872 PubMed 12567263 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
34 nlx_152872 PubMed 12011157 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
35 nlx_152872 PubMed 12676897 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
36 nlx_152872 PubMed 17564961 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
37 nlx_152872 PubMed 18587492 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
38 nlx_152872 PubMed 19262743 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
39 nlx_152872 PubMed 19633732 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
40 nlx_152872 PubMed 19668596 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
41 nlx_152872 PubMed 20508808 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
42 nlx_152872 PubMed 21031598 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
43 nlx_152872 PubMed 21552497 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
44 nlx_152872 PubMed 21866214 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
45 nlx_152872 PubMed 22219628 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
46 nlx_152872 PubMed 22669729 A relationship between CRYGD and the N/AADcataract 4, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
47 nlx_152872 PubMed 16141006 A relationship between CRYGS and the N/AADcataract 20, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
48 nlx_152872 PubMed 18587492 A relationship between CRYGS and the N/AADcataract 20, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
49 nlx_152872 PubMed 19262743 A relationship between CRYGS and the N/AADcataract 20, multiple types was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
50 nlx_152872 PubMed 12471561 A relationship between CRYM and the PediatricADdeafness, autosomal dominant 40 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
51 nlx_152872 PubMed 16523341 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
52 nlx_152872 PubMed 19153373 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
53 nlx_152872 PubMed 22197934 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
54 nlx_152872 PubMed 22843259 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
55 nlx_152872 PubMed 23698128 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
56 nlx_152872 PubMed 30982608 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
57 nlx_152872 PubMed 30982609 A relationship between CSF1R and the N/AAD/ARleukoencephalopathy, diffuse hereditary, with spheroids; brain abnormalities, neurodegeneration, and dysosteosclerosis was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
58 nlx_152872 PubMed 18955567 A relationship between CSF2RA and the PediatricXLsurfactant metabolism dysfunction, pulmonary, 4 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
59 nlx_152872 PubMed 18955570 A relationship between CSF2RA and the PediatricXLsurfactant metabolism dysfunction, pulmonary, 4 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
60 nlx_152872 PubMed 20622029 A relationship between CSF2RA and the PediatricXLsurfactant metabolism dysfunction, pulmonary, 4 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
61 nlx_152872 PubMed 9410898 A relationship between CSF2RB and the PediatricARsurfactant metabolism dysfunction, pulmonary, 5 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
62 nlx_152872 PubMed 21075760 A relationship between CSF2RB and the PediatricARsurfactant metabolism dysfunction, pulmonary, 5 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
63 nlx_152872 PubMed 4825608 A relationship between CSF3R and the PediatricARneutropenia, severe congenital, 7, autosomal recessive was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
64 nlx_152872 PubMed 19620628 A relationship between CSF3R and the PediatricARneutropenia, severe congenital, 7, autosomal recessive was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
65 nlx_152872 PubMed 24753537 A relationship between CSF3R and the PediatricARneutropenia, severe congenital, 7, autosomal recessive was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
66 nlx_152872 PubMed 26324699 A relationship between CSF3R and the PediatricARneutropenia, severe congenital, 7, autosomal recessive was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
67 nlx_152872 PubMed 15800623 A relationship between CSNK1D and the N/AADadvanced sleep phase syndrome, familial, 2 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
68 nlx_152872 PubMed 23636092 A relationship between CSNK1D and the N/AADadvanced sleep phase syndrome, familial, 2 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
69 nlx_152872 PubMed 27048600 A relationship between CSNK2A1 and the PediatricADokur-chung neurodevelopmental syndrome was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
70 nlx_152872 PubMed 28725024 A relationship between CSNK2A1 and the PediatricADokur-chung neurodevelopmental syndrome was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
71 nlx_152872 PubMed 29240241 A relationship between CSNK2A1 and the PediatricADokur-chung neurodevelopmental syndrome was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
72 nlx_152872 PubMed 29383814 A relationship between CSNK2A1 and the PediatricADokur-chung neurodevelopmental syndrome was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
73 nlx_152872 PubMed 29619237 A relationship between CSNK2A1 and the PediatricADokur-chung neurodevelopmental syndrome was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
74 nlx_152872 PubMed 24360803 A relationship between CSPP1 and the N/AARjeune asphyxiating thoracic dystrophy; joubert syndrome 21 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
75 nlx_152872 PubMed 24360807 A relationship between CSPP1 and the N/AARjeune asphyxiating thoracic dystrophy; joubert syndrome 21 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
76 nlx_152872 PubMed 24360808 A relationship between CSPP1 and the N/AARjeune asphyxiating thoracic dystrophy; joubert syndrome 21 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
77 nlx_152872 PubMed 12507422 A relationship between CSRP3 and the PediatricADcardiomyopathy, familial hypertrophic 12; cardiomyopathy, dilated, 1m was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
78 nlx_152872 PubMed 14567970 A relationship between CSRP3 and the PediatricADcardiomyopathy, familial hypertrophic 12; cardiomyopathy, dilated, 1m was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
79 nlx_152872 PubMed 12642359 A relationship between CSRP3 and the PediatricADcardiomyopathy, familial hypertrophic 12; cardiomyopathy, dilated, 1m was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
80 nlx_152872 PubMed 18505755 A relationship between CSRP3 and the PediatricADcardiomyopathy, familial hypertrophic 12; cardiomyopathy, dilated, 1m was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
81 nlx_152872 PubMed 20087448 A relationship between CSRP3 and the PediatricADcardiomyopathy, familial hypertrophic 12; cardiomyopathy, dilated, 1m was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
82 nlx_152872 PubMed 22429680 A relationship between CSRP3 and the PediatricADcardiomyopathy, familial hypertrophic 12; cardiomyopathy, dilated, 1m was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
83 nlx_152872 PubMed 4655034 A relationship between CST3 and the N/AADcerebral amyloid angiopathy was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
84 nlx_152872 PubMed 3495457 A relationship between CST3 and the N/AADcerebral amyloid angiopathy was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
85 nlx_152872 PubMed 2900981 A relationship between CST3 and the N/AADcerebral amyloid angiopathy was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
86 nlx_152872 PubMed 11760381 A relationship between CST3 and the N/AADcerebral amyloid angiopathy was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
87 nlx_152872 PubMed 16612982 A relationship between CST3 and the N/AADcerebral amyloid angiopathy was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
88 nlx_152872 PubMed 18566660 A relationship between CST3 and the N/AADcerebral amyloid angiopathy was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
89 nlx_152872 PubMed 21944047 A relationship between CSTA and the N/AARpeeling skin syndrome 4 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
90 nlx_152872 PubMed 25400170 A relationship between CSTA and the N/AARpeeling skin syndrome 4 was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
91 nlx_152872 PubMed 6137660 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
92 nlx_152872 PubMed 8596935 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
93 nlx_152872 PubMed 9012407 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
94 nlx_152872 PubMed 9054946 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
95 nlx_152872 PubMed 9126745 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
96 nlx_152872 PubMed 9090386 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
97 nlx_152872 PubMed 9527146 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
98 nlx_152872 PubMed 9529356 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
99 nlx_152872 PubMed 9814834 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link
100 nlx_152872 PubMed 9932979 A relationship between CSTB and the N/AARmyoclonic epilepsy of unverricht and lundborg was found in this paper by the NHGRI clinical genomic database. Data: Gene Annotation Link