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Search results for dicer1

561 hits were found for dicer1

# Family MCID Name MIFTS Score
1
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 143.178
2
INH023 Inherited Cancer-Predisposing Syndrome 53 143.178
3
DCR010 Dicer1 Tumor Predisposition 31 137.562
5
P PLR004 Pleuropulmonary Blastoma 65 125.902
6
P TMR010 Tumor Predisposition Syndrome 69 74.053
7
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 41 37.445
8
GLB024 Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor 31 33.270
9
c RHB021 Rhabdomyosarcoma, Embryonal, 2 23 31.556
10
P RHB003 Rhabdomyosarcoma 66 30.844
11
P PNB001 Pineoblastoma 49 27.394
12
GTR002 Goiter 52 20.409
13
NPH113 Nephroma 37 18.495
14
P EMB005 Embryonal Rhabdomyosarcoma 53 17.233
15
SRT003 Sertoli-Leydig Cell Tumor 38 17.063
16
GYN003 Gynandroblastoma 24 16.996
17
P CLR023 Colorectal Cancer 100 16.107
18
P MLT008 Multinodular Goiter 42 15.294
19
SRC014 Sarcoma 64 15.226
20
P OVR042 Ovarian Cancer 88 13.993
21
PLM032 Pulmonary Blastoma 47 13.906
22
P MDL005 Medulloblastoma 75 12.842
23
P NRB001 Neuroblastoma 66 12.324
25
MYL009 Myelodysplastic Syndrome 67 10.873
26
MDL002 Medulloepithelioma 39 10.676
27
SPR008 Supratentorial Primitive Neuroectodermal Tumor 42 10.563
28
EMB002 Embryoma 37 10.207
29
DFF036 Differentiated Thyroid Carcinoma 51 10.180
30
PST028 Post-Traumatic Stress Disorder 59 10.131
31
c WLM013 Wilms Tumor 1 65 10.031
32
MCR013 Microphthalmia 60 9.878
33
THY123 Thyroid Gland Follicular Carcinoma 53 9.282
34
P FRG001 Fragile X Syndrome 70 9.006
35
WLL022 Well-Differentiated Fetal Adenocarcinoma of the Lung 17 8.931
36
SXC001 Sex Cord-Gonadal Stromal Tumor 47 8.795
37
MLG154 Malignant Sertoli-Leydig Cell Tumor of the Ovary 25 8.412
38
KDN019 Kidney Sarcoma 26 8.349
39
c LKM061 Leukemia, Acute Myeloid 83 7.904
40
OVR121 Ovarian Sex-Cord Stromal Tumor 31 7.675
41
c JVN002 Juvenile Type Testicular Granulosa Cell Tumor 34 7.568
42
WLM012 Wilms Tumor Predisposition 23 7.568
43
MLG155 Maligant Granulosa Cell Tumor of the Ovary 15 7.393
44
P RTN008 Retinitis Pigmentosa 79 7.354
45
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 28 7.191
46
P PLM064 Pulmonary Sequestration 22 7.191
47
MCR379 Microcystic Stromal Tumor 29 7.191
48
P LKM071 Leukemia, Chronic Lymphocytic 74 7.163
49
PNL014 Pineal Gland Cancer 40 7.138
50
LYD001 Leydig Cell Tumor 45 6.979
51
P CRN038 Carney Complex Variant 63 6.763
52
DGR001 Digeorge Syndrome 62 6.705
53
CRT002 Cartilage-Hair Hypoplasia 60 6.488
54
P BTR001 Botryoid Rhabdomyosarcoma 36 6.488
55
KDN025 Kidney Cortex Disease 17 6.368
56
c ATR065 Atrial Septal Defect 8 33 6.368
57
c DYS059 Dystonia 16 47 6.368
58
DSS008 Disease of Mental Health 74 6.368
59
MLT180 Multisystem Inflammatory Syndrome in Children 33 6.368
60
EXC001 Exocervical Carcinoma 21 6.368
61
BLD023 Bladder Leiomyoma 32 6.368
62
KDN016 Kidney Benign Neoplasm 30 6.368
63
CRV028 Cervical Adenosarcoma 32 6.368
64
PLR022 Pleural Disease 45 6.368
65
SKL003 Skeletal Muscle Cancer 29 6.368
66
P TST016 Testicular Granulosa Cell Tumor 28 6.368
67
c CNG405 Congenital Pulmonary Airway Malformation Type 4 11 6.368
68
THY029 Thyroid Carcinoma 54 6.090
69
END057 Endometrial Cancer 71 5.707
70
P BRS047 Breast Cancer 97 5.575
71
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 4.972
72
P GST053 Gastric Cancer 82 4.509
73
SPN035 Spindle Cell Sarcoma 51 4.418
74
c RHB023 Rhabdomyosarcoma, Embryonal, 1 45 3.868
75
c THY109 Thyroid Cancer, Nonmedullary, 1 55 3.635
76
P LNG064 Lung Cancer Susceptibility 3 70 3.522
77
P RRT020 Rare Tumor 39 3.435
78
ADN018 Adenoma 58 3.429
79
CLN015 Colon Adenocarcinoma 64 3.358
80
GST103 Gastric Cancer, Hereditary Diffuse 68 3.309
81
BLD173 Bladder Small Cell Carcinoma 44 3.254
82
END041 Endometrial Adenocarcinoma 63 3.235
83
SML009 Small Intestine Adenocarcinoma 57 3.174
84
P ADN016 Adenocarcinoma 63 3.141
85
P PRS040 Prostate Cancer 95 2.994
86
c CLR087 Colorectal Cancer 12 34 2.961
87
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 2.961
88
LNG039 Lung Squamous Cell Carcinoma 57 2.956
89
GST040 Gastric Adenocarcinoma 66 2.830
90
P LNG032 Lung Cancer 98 2.827
91
ADN011 Adenoid Cystic Carcinoma 68 2.708
92
ADN020 Adenosarcoma 41 2.633
93
AMN001 Amenorrhea 53 2.622
94
ADN089 Adenosquamous Lung Carcinoma 49 2.589
95
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 2.589
96
CRC021 Carcinosarcoma 62 2.574
97
P HYP086 Hypothyroidism 69 2.413
98
P TRT010 Teratoma 50 2.375
99
GLM045 Glioma 62 2.244
100
c MSM022 Mismatch Repair Cancer Syndrome 1 69 2.229
101
LYM133 Lymphoma, Hodgkin, Classic 74 2.219
102
P GLM040 Glioma Susceptibility 1 70 2.199
103
P OVR082 Overgrowth Syndrome 42 2.187
104
INT176 Intraocular Medulloepithelioma 14 2.090
105
PPL022 Papilloma 53 2.078
106
PPL002 Papillary Carcinoma 46 2.078
107
SQM002 Squamous Cell Papilloma 45 2.060
108
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.016
109
P LYM118 Lymphoma 69 2.002
110
ESP021 Esophageal Cancer 84 1.983
111
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.858
112
SKN022 Skin Squamous Cell Carcinoma 54 1.858
113
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.858
114
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.812
115
RHB001 Rhabdoid Cancer 68 1.806
116
P BLD134 Bladder Cancer 79 1.803
117
P PTT006 Pituitary Adenoma 55 1.771
118
P LFR001 Li-Fraumeni Syndrome 73 1.755
119
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 1.750
120
P EPN001 Ependymoblastoma 44 1.728
121
P FBR017 Fibrosarcoma 55 1.726
122
P NRF002 Neurofibromatosis 60 1.726
123
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.694
124
P HPT021 Hepatitis 68 1.673
125
PTT037 Pituitary Tumors 44 1.649
126
P INF032 Infertility 60 1.648
127
PPL058 Papilloma of Choroid Plexus 54 1.641
128
ATY002 Atypical Choroid Plexus Papilloma 23 1.641
129
P MLN007 Male Infertility 56 1.560
130
AGN016 Aging 54 1.535
131
c BSL007 Basal Cell Carcinoma 68 1.532
132
THY124 Thyroid Gland Papillary Carcinoma 38 1.530
133
RHB024 Rhabdomyosarcoma 2 65 1.517
134
CYS044 Cystic Disease of Lung 19 1.483
135
P CNR004 Cone-Rod Dystrophy 2 75 1.479
136
CNT045 Central Nervous System Sarcoma 23 1.444
137
CLB026 Colobomatous Microphthalmia 46 1.438
138
SPN009 Spindle Cell Rhabdomyosarcoma 40 1.436
139
THY030 Thyroid Gland Disease 50 1.425
140
SFT003 Soft Tissue Sarcoma 57 1.425
141
P NSP012 Nasopharyngeal Carcinoma 60 1.417
142
P HPT023 Hepatocellular Carcinoma 95 1.379
143
c GLM043 Glioma Susceptibility 9 30 1.351
144
c GLM047 Glioma Susceptibility 3 32 1.351
145
c GLM025 Glioma Susceptibility 2 29 1.351
146
P OLG002 Oligodendroglioma 66 1.351
147
MNN043 Meningioma, Familial 79 1.351
148
OST159 Osteogenic Sarcoma 66 1.346
149
PLM026 Pilomatrixoma 57 1.311
150
AZS001 Azoospermia 45 1.306
151
ORL011 Oral Cancer 60 1.278
152
CLR030 Clear Cell Renal Cell Carcinoma 54 1.268
153
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.260
154
OVR094 Ovarian Epithelial Cancer 39 1.233
155
BRS099 Breast Ductal Carcinoma 61 1.228
156
NDL007 Nodular Goiter 48 1.222
157
P KDN017 Kidney Cancer 60 1.217
158
P RHM011 Rheumatoid Arthritis 81 1.182
159
P ART022 Arthritis 70 1.182
160
47X002 47,xyy 48 1.182
161
PPL004 Papillary Squamous Carcinoma 39 1.178
162
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.164
163
P ADL099 Adult Cystic Nephroma 24 1.144
164
ACT084 Acute Stress Disorder 53 1.124
165
P RCT021 Rectum Cancer 54 1.124
166
P HYP265 Hypotonia 42 1.124
167
P ALZ034 Alzheimer Disease 87 1.115
168
THY111 Thyroid Carcinoma, Familial Medullary 67 1.084
169
PNM008 Pneumothorax 54 1.084
170
CNN003 Conn's Syndrome 77 1.084
171
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.084
172
THY125 Thyroid Gland Medullary Carcinoma 48 1.084
173
P RTN024 Retinoblastoma 72 1.076
174
LNG012 Lung Occult Squamous Cell Carcinoma 20 1.035
175
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 1.035
176
NPH003 Nephrocalcinosis 49 1.033
177
NPH009 Nephrolithiasis 54 1.033
178
ADR016 Adrenal Cortical Carcinoma 61 1.018
179
c PRC016 Pre-Eclampsia 64 1.002
180
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.002
181
ADR004 Adrenal Cortical Adenocarcinoma 38 1.002
182
THY128 Thyroid Tumor 33 1.002
183
EWN003 Ewing Sarcoma 70 0.997
184
NRR001 Neuroretinitis 42 0.986
185
P FML011 Familial Adenomatous Polyposis 71 0.986
186
FLL031 Follicular Adenoma 40 0.986
187
UTR024 Uterine Carcinosarcoma 58 0.986
188
RTN023 Retinitis 45 0.986
189
RHB019 Rhabdomyosarcoma of the Cervix Uteri 13 0.986
190
IMM003 Immunoglobulin Alpha Deficiency 44 0.964
191
MRK001 Merkel Cell Carcinoma 65 0.955
192
CRB074 Cerebral Sarcoma 15 0.952
193
FTT001 Fatty Liver Disease 61 0.952
194
P BCL017 B-Cell Lymphoma 57 0.933
195
ADN028 Adenosarcoma of the Uterus 18 0.933
196
DFF005 Diffuse Large B-Cell Lymphoma 55 0.914
197
NNL006 Non-Alcoholic Steatohepatitis 54 0.914
198
UTR056 Uterine Corpus Endometrial Carcinoma 27 0.914
199
P RSP003 Respiratory Failure 74 0.914
200
P END044 Endometriosis 62 0.914
201
RCT020 Rectum Adenocarcinoma 48 0.914
202
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.914
203
PLM033 Pulmonary Embolism 58 0.914
204
SQM006 Squamous Cell Carcinoma 59 0.899
205
TRD003 Taurodontism 30 0.894
206
c SPR162 Spermatogenic Failure 50 42 0.894
207
HRW001 Hair Whorl 35 0.894
208
P CWD010 Cowden Syndrome 71 0.894
209
P MYL006 Myeloid Leukemia 60 0.894
210
GLL048 Glial Tumor 52 0.894
211
P PRD008 Periodontitis 64 0.894
212
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.894
213
c LKM005 Leukemia, T-Cell, Chronic 33 0.894
214
P PNC035 Pancreatic Cancer 86 0.888
215
CYS021 Cystic Adenomatoid Malformation of Lung 32 0.887
216
ADL002 Adult Syndrome 69 0.878
217
c THY102 Thyroid Cancer, Nonmedullary, 2 54 0.878
218
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.878
219
c NRF024 Neurofibromatosis, Type I 76 0.878
220
PNM010 Pneumothorax, Primary Spontaneous 58 0.878
221
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 0.878
222
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.878
223
P CYS039 Cystic Kidney Disease 52 0.878
224
PPL001 Papillary Adenoma 44 0.878
225
P ACT010 Acth-Secreting Pituitary Adenoma 60 0.878
226
SKN023 Skin Tag 41 0.878
227
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.878
228
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.872
229
CLT003 Colitis 63 0.872
230
P OVR046 Ovarian Cyst 44 0.872
231
P LKM002 Leukemia 66 0.872
232
MTH009 Mouth Disease 57 0.872
233
MSN004 Mesenchymal Cell Neoplasm 42 0.872
234
P EYD002 Eye Disease 57 0.872
235
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.872
236
LNG099 Lung Disease 62 0.859
237
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.858
238
MLG169 Malignant Astrocytoma 57 0.848
239
P THR014 Thrombocytopenia 66 0.848
240
THY122 Thyroid Gland Cancer 59 0.848
241
SRT002 Sertoli Cell Tumor 38 0.848
242
SMN007 Seminoma 42 0.848
243
HYP266 Hypoxia 56 0.848
244
BSL036 Basal Cell Nevus Syndrome 73 0.823
245
MYL069 Myeloma, Multiple 77 0.823
246
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.823
247
ANG020 Angiosarcoma 63 0.823
248
P PLG001 Pelger-Huet Anomaly 52 0.823
249
P PLM036 Pulmonary Fibrosis 65 0.823
250
CHR178 Chromosomal Triplication 34 0.823
251
END086 End Stage Renal Disease 54 0.823
252
EMB007 Embryonal Sarcoma 40 0.823
253
LMN016 Luminal Breast Carcinoma B 28 0.821
254
P LMN015 Luminal Breast Carcinoma a 34 0.821
255
P BLD062 Bile Duct Cancer 68 0.821
256
OVR062 Ovary Serous Adenocarcinoma 25 0.821
257
PRM126 Primary Peritoneal Carcinoma 61 0.821
258
c PRS070 Prostate Cancer, Hereditary, 12 22 0.797
259
c PRS071 Prostate Cancer, Hereditary, 13 25 0.797
260
c PRS117 Prostate Cancer, Hereditary, 11 24 0.797
261
c PRS114 Prostate Cancer, Hereditary, 2 33 0.797
262
c PRS097 Prostate Cancer, Hereditary, 1 38 0.797
263
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.797
264
RCK004 Rickets 65 0.795
265
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.795
266
STM007 Stomatitis 52 0.795
267
CLR003 Clear Cell Adenocarcinoma 50 0.795
268
SPN186 Spinal Cord Injury 61 0.795
269
PNC056 Pineocytoma 44 0.770
270
c SML038 Small Cell Cancer of the Lung 69 0.763
271
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.763
272
GLB002 Glioblastoma 67 0.763
273
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 22 0.763
274
P RTN016 Retinal Degeneration 52 0.763
275
FTL048 Fetal Lung Interstitial Tumor 13 0.740
276
CRP032 Corpus Callosum, Agenesis of 49 0.725
277
P KLZ004 Kala-Azar 1 41 0.725
278
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.725
279
LYM040 Lymphoblastic Lymphoma 53 0.725
280
P HYD006 Hydrocephalus 63 0.725
281
P INS002 in Situ Carcinoma 53 0.725
282
VSC003 Visceral Leishmaniasis 54 0.725
283
LMY003 Leiomyomatosis 43 0.725
284
INT020 Intravenous Leiomyomatosis 36 0.725
285
LSH001 Leishmaniasis 63 0.725
286
FHT001 Fh Tumor Predisposition Syndrome 26 0.725
287
GRM010 Germ Cells Tumors 33 0.720
288
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.690
289
OVR044 Ovarian Carcinosarcoma 46 0.690
290
KDN007 Kidney Clear Cell Sarcoma 40 0.690
291
GNG008 Ganglioneuroblastoma 46 0.676
292
ECT002 Ectomesenchymoma 31 0.676
293
RDT005 Radiation Induced Cancer 21 0.676
294
c BSL024 Basal Cell Carcinoma 1 54 0.661
295
c BSL034 Basal Cell Carcinoma 7 25 0.661
296
RMB001 Rombo Syndrome 29 0.661
297
BSL044 Basal Cell Carcinoma, Infundibulocystic 35 0.661
298
P TRC095 Trichoepithelioma, Multiple Familial, 1 32 0.661
299
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.661
300
NDL009 Nodular Basal Cell Carcinoma 40 0.661
301
MTT001 Metatypical Basal Cell Carcinoma 31 0.661
302
PGM002 Pigmented Basal Cell Carcinoma 31 0.661
303
ANL013 Anal Margin Basal Cell Carcinoma 18 0.661
304
SBC013 Sebaceous Basal Cell Carcinoma 13 0.661
305
MCR016 Micronodular Basal Cell Carcinoma 34 0.661
306
ADM002 Adamantinoid Basal Cell Epithelioma 20 0.661
307
CLR015 Clear Cell Basal Cell Carcinoma 39 0.661
308
ADN015 Adenoid Basal Cell Carcinoma 31 0.661
309
INF027 Infiltrative Basal Cell Carcinoma 32 0.661
310
CYS004 Cystic Basal Cell Carcinoma 36 0.661
311
SRC003 Sarcomatoid Basal Cell Carcinoma 28 0.661
312
SGN001 Signet Ring Basal Cell Carcinoma 32 0.661
313
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.661
314
9Q2001 9q22.3 Microdeletion 24 0.661
315
LNR004 Linear Porokeratosis 33 0.661
316
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 16 0.661
317
CRC045 Carcinoma of Gallbladder and Extrahepatic Biliary Tract 20 0.661
318
VNH007 Von Hippel-Lindau Syndrome 73 0.652
319
ESP027 Esophagus Squamous Cell Carcinoma 45 0.630
320
BRT002 Birt-Hogg-Dube Syndrome 64 0.621
321
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.621
322
ACT088 Acute Insulin Response 39 0.621
323
SRC027 Sarcoma, Synovial 58 0.621
324
P OPT006 Optic Nerve Disease 57 0.621
325
LNG031 Lung Benign Neoplasm 51 0.621
326
GST019 Gastrointestinal Stromal Tumor 78 0.607
327
PRL032 Perlman Syndrome 57 0.601
328
c WLM011 Wilms Tumor 6 25 0.601
329
ANT039 Antisynthetase Syndrome 55 0.601
330
c WLM018 Wilms Tumor 5 54 0.601
331
GRM005 Germ Cell Cancer 46 0.601
332
P TST048 Testicular Sex Cord-Stromal Neoplasm 24 0.601
333
CNT033 Central Nervous System Cancer 47 0.601
334
P NRV006 Nervous System Cancer 47 0.601
335
CHL018 Childhood Medulloblastoma 47 0.601
336
MLG055 Malignant Cystic Nephroma 9 0.601
337
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.601
338
MYL005 Myelofibrosis 70 0.573
339
DST001 Distal Biliary Tract Carcinoma 24 0.488
340
ACR014 Acral Lentiginous Melanoma 52 0.488
341
P EPT012 Epithelioid Sarcoma 41 0.488
342
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.488
343
VGN017 Vaginal Cancer 58 0.488
344
LBL001 Lobular Neoplasia 55 0.488
345
CRV038 Cervical Squamous Cell Carcinoma 56 0.488
346
c ALB010 Albinism, Oculocutaneous, Type Ib 52 0.488
347
P LNG021 Lung Occult Small Cell Carcinoma 20 0.488
348
DSM007 Desmoplastic Small Round Cell Tumor 54 0.488
349
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 27 0.488
350
PLM001 Pulmonary Tuberculosis 69 0.471
351
IRN008 Iron Overload in Africa 51 0.445
352
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.445
353
RJS001 Ruijs-Aalfs Syndrome 47 0.445
354
HPT079 Hepatoid Adenocarcinoma 39 0.445
355
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.445
356
c HPT073 Hepatitis C Virus 71 0.445
357
RNL119 Renal Cell Carcinoma, Xp11-Associated 42 0.445
358
ADL096 Adult Hepatocellular Carcinoma 60 0.445
359
MTN001 Metanephric Adenoma 39 0.445
360
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.445
361
PDT042 Pediatric Hepatocellular Carcinoma 50 0.445
362
PTY007 Pityriasis Rotunda 26 0.445
363
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.445
364
FBR086 Fibrolamellar Carcinoma 59 0.445
365
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.445
366
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.445
367
NSP002 Nasopharyngitis 45 0.395
368
P MLT074 Multiple Endocrine Neoplasia 58 0.376
369
c TYP009 Type 2 Diabetes Mellitus 92 0.337
370
P DBT009 Diabetes Mellitus 67 0.337
371
P SCH015 Schizophrenia 74 0.315
372
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.315
373
MCC012 Mccune-Albright Syndrome 69 0.315
374
PTZ001 Peutz-Jeghers Syndrome 69 0.315
375
ALL006 Allergic Asthma 56 0.315
376
ART140 Arteries, Anomalies of 52 0.292
377
LPP008 Lipoprotein Quantitative Trait Locus 65 0.292
378
P SML001 Small Cell Carcinoma 52 0.292
379
ACT162 Acute Sensory Ataxic Neuropathy 24 0.292
380
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.266
381
P ATX030 Ataxia-Telangiectasia 80 0.266
382
CHR525 Chromosome Xq26.3 Duplication Syndrome 36 0.266
383
OVR058 Ovarian Small Cell Carcinoma 39 0.266
384
TLN003 Telangiectasis 51 0.266
385
SKN019 Skin Melanoma 70 0.266
386
FML168 Familial Isolated Pituitary Adenoma 32 0.266
387
WRN001 Werner Syndrome 69 0.238
388
BCT022 Bacterial Infectious Disease 56 0.238
389
P CRB045 Cerebellar Hypoplasia 40 0.238
390
ENC044 Enchondromatosis, Multiple, Ollier Type 56 0.238
391
c MLT086 Multiple Endocrine Neoplasia, Type Iv 50 0.238
392
MLT145 Multiple Enchondromatosis, Maffucci Type 49 0.238
393
c LFR007 Li-Fraumeni Syndrome 2 44 0.238
394
FML211 Familial Papillary or Follicular Thyroid Carcinoma 25 0.238
395
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.206
396
FBR054 Fibroma 44 0.206
397
c MJR024 Major Affective Disorder 9 40 0.206
398
c MJR022 Major Affective Disorder 8 37 0.206
399
c THR092 Thrombophilia Due to Thrombin Defect 74 0.206
400
ECT026 Ectopic Pregnancy 47 0.206
401
P PRG013 Paraganglioma 57 0.206
402
P TBR001 Tuberous Sclerosis 69 0.206
403
P MLN008 Melanoma 75 0.206
404
P LVR013 Liver Disease 68 0.206
405
P LYN001 Lynch Syndrome 76 0.206
406
DYS101 Dysgerminoma 44 0.206
407
P BPL003 Bipolar Disorder 56 0.206
408
KRN002 Kearns-Sayre Syndrome 63 0.206
409
c MLG081 Malignant Teratoma 37 0.206
410
GND001 Gonadoblastoma 43 0.168
411
HYP865 Hypogonadotropic Hypogonadism 25 with Anosmia 23 0.168
412
DSS032 Disease by Infectious Agent 55 0.168
413
END062 Endometrial Hyperplasia 48 0.168
414
P OST002 Osteoporosis 77 0.168
415
ADR040 Adrenal Gland Pheochromocytoma 45 0.168
416
P MYC084 Mycobacterium Tuberculosis 1 68 0.168
417
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.168
418
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.168
419
P PHC003 Pheochromocytoma 70 0.168
420
c SPN294 Spinocerebellar Ataxia 1 53 0.168
421
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.168
422
c FML346 Familial Adenomatous Polyposis 1 65 0.168
423
c TBR025 Tuberous Sclerosis 1 84 0.168
424
EMB018 Embryonal Tumor with Multilayered Rosettes, C19mc-Altered 10 0.168
425
ADL025 Adult Pineoblastoma 20 0.168
426
SVR004 Severe Combined Immunodeficiency 71 0.168
427
ADN012 Adenocarcinoma in Situ 42 0.168
428
ACR007 Acromegaly 70 0.168
429
P LRY044 Larynx Cancer 53 0.168
430
BRN028 Brain Cancer 73 0.168
431
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.168
432
P GND004 Gonadal Dysgenesis 46 0.168
433
MDD011 Mood Disorder 62 0.168
434
VRL018 Virilizing Ovarian Tumor 11 0.168
435
ALD013 Aldosterone-Producing Adenoma 36 0.168
436
CYT002 Cytokine Deficiency 43 0.168
437
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 0.168
438
ALL014 Allergic Encephalomyelitis 34 0.168
439
EXP004 Exophthalmos 50 0.168
440
GGN002 Gigantism 33 0.168
441
PPL050 Papillary Tumor of the Pineal Region 31 0.168
442
c NRF023 Neurofibromatosis, Type Ii 70 0.119
443
P BCK002 Beckwith-Wiedemann Syndrome 61 0.119
444
CYS001 Cystic Fibrosis 77 0.119
445
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.119
446
c SPR119 Spermatogenic Failure, X-Linked, 1 36 0.119
447
c OTP006 Otopalatodigital Syndrome, Type I 60 0.119
448
PRS129 Prostatic Hyperplasia, Benign 48 0.119
449
WVR001 Weaver Syndrome 56 0.119
450
P SPP010 Suppressor of Tumorigenicity 3 51 0.119
451
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 65 0.119
452
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.119
453
DWN001 Down Syndrome 70 0.119
454
c BRN108 Branchiootic Syndrome 1 63 0.119
455
P LKM062 Leukemia, Acute Lymphoblastic 69 0.119
456
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.119
457
FCL009 Focal Dermal Hypoplasia 64 0.119
458
DTS001 Diets-Jongmans Syndrome 22 0.119
459
c THY100 Thyroid Cancer, Nonmedullary, 4 18 0.119
460
P ADL017 Adult T-Cell Leukemia 54 0.119
461
c PCH010 Pachyonychia Congenita 3 43 0.119
462
LWG006 Low Grade Glioma 41 0.119
463
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.119
464
P PLY014 Polycystic Kidney Disease 71 0.119
465
FBR009 Fibrous Dysplasia 48 0.119
466
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.119
467
c CRN243 Carney Complex, Type 1 53 0.119
468
ALC007 Alcohol Dependence 65 0.119
469
c ATR087 Atrial Standstill 1 74 0.119
470
c SPN225 Spondyloarthropathy 1 70 0.119
471
ATH013 Atherosclerosis Susceptibility 63 0.119
472
CST001 Costello Syndrome 68 0.119
473
c FNC027 Fanconi Anemia, Complementation Group a 81 0.119
474
IMM167 Immune Deficiency Disease 77 0.119
475
MCS004 Mucosal Melanoma 46 0.119
476
P ATR011 Atrial Fibrillation 66 0.119
477
P BRT040 Baraitser-Winter Syndrome 34 0.119
478
TRC097 Tracheomalacia 43 0.119
479
CLR108 Colorectal Adenoma 63 0.119
480
PRT010 Parathyroid Carcinoma 68 0.119
481
c FNC029 Fanconi Anemia, Complementation Group I 55 0.119
482
P ESP035 Esophagitis, Eosinophilic, 1 57 0.119
483
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.119
484
LYM007 Lymphangioleiomyomatosis 68 0.119
485
JVN004 Juvenile Myelomonocytic Leukemia 67 0.119
486
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.119
487
LMY014 Leiomyoma, Uterine 55 0.119
488
P MLN066 Melanoma, Cutaneous Malignant 1 66 0.119
489
PPL052 Papillomatosis, Confluent and Reticulated 34 0.119
490
P NNN008 Noonan Syndrome 1 76 0.119
491
P CFF008 Coffin-Siris Syndrome 1 63 0.119
492
P OCY003 Oocyte Maturation Defect 1 46 0.119
493
c PRK058 Parkinson Disease 16 18 0.119
494
P MTR004 Maturity-Onset Diabetes of the Young 66 0.119
495
BLM001 Bloom Syndrome 65 0.119
496
P SJG008 Sjogren Syndrome 61 0.119
497
c HYP864 Hypoparathyroidism, Familial Isolated, 1 30 0.119
498
P TTR001 Tetralogy of Fallot 69 0.119
499
OST017 Osteomyelitis 63 0.119
500
P BND020 Bone Disease 60 0.119
501
P NPH005 Nephronophthisis 59 0.119
502
LMY002 Leiomyoma 51 0.119
503
GT001 Gout 63 0.119
504
SVR001 Severe Acute Respiratory Syndrome 68 0.119
505
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.119
506
PRS021 Prostatic Adenoma 43 0.119
507
OVR015 Ovarian Mixed Germ Cell Neoplasm 35 0.119
508
BLD050 Bladder Urachal Carcinoma 24 0.119
509
LYM027 Lymphopenia 56 0.119
510
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 0.119
511
URT010 Ureteral Obstruction 45 0.119
512
SPN051 Spondylitis 51 0.119
513
URM002 Uremia 47 0.119
514
PRS045 Prostatic Hypertrophy 52 0.119
515
MYL031 Myeloproliferative Neoplasm 66 0.119
516
NRN004 Neuroendocrine Tumor 55 0.119
517
CYS009 Cystadenoma 43 0.119
518
P CRN025 Corneal Dystrophy 49 0.119
519
NVS001 Neovascular Glaucoma 52 0.119
520
P HYP024 Hypoparathyroidism 55 0.119
521
P ESP024 Esophagitis 60 0.119
522
P HYP061 Hypertrophic Cardiomyopathy 69 0.119
523
HMS001 Hemosiderosis 48 0.119
524
INF009 Inflammatory Spondylopathy 30 0.119
525
P GRV001 Graves' Disease 54 0.119
526
FCH001 Fuchs' Endothelial Dystrophy 48 0.119
527
HYP043 Hyperandrogenism 47 0.119
528
GST033 Gestational Diabetes 61 0.119
529
LKC002 Leukocoria 33 0.119
530
SKN016 Skin Disease 62 0.119
531
P RST002 Restrictive Cardiomyopathy 54 0.119
532
INT066 Interstitial Lung Disease 60 0.119
533
VCC001 Vaccinia 49 0.119
534
PSY004 Psychotic Disorder 66 0.119
535
TRT001 Teratocarcinoma 41 0.119
536
CNC002 Cinca Syndrome 65 0.119
537
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.119
538
CRT024 Cartilage-Hair Hypoplasia - Anauxetic Dysplasia Spectrum Disorders 13 0.119
539
ACT250 Acute Megakaryocytic Leukemia 63 0.119
540
FNC007 Functioning Pituitary Adenoma 42 0.119
541
CLF001 Cleft Lip 54 0.119
542
DYS017 Dysgerminoma of Ovary 37 0.119
543
CLR017 Clear Cell Sarcoma 44 0.119
544
DFF016 Diffuse Astrocytoma 48 0.119
545
FML008 Familial Retinoblastoma 49 0.119
546
MCP006 Mucoepidermoid Carcinoma 48 0.119
547
P RCR004 Recurrent Respiratory Papillomatosis 48 0.119
548
c CNG023 Congenital Fibrosarcoma 42 0.119
549
SML041 Small-Cell Carcinoma of the Ovary of Hypercalcemic Type 36 0.119
550
P HYP076 Hyperthyroidism 53 0.119
551
P ORL007 Oral Cavity Cancer 52 0.119
552
c PSD047 Pseudo-Turner Syndrome 52 0.119
553
MXD032 Mixed Germ Cell Tumor 24 0.119
554
P RRH023 Rare Hereditary Hemochromatosis 53 0.119
555
P CNG396 Congenital Pulmonary Airway Malformation Type 2 13 0.119
556
c CNG398 Congenital Pulmonary Airway Malformation Type 1 12 0.119
557
OVR098 Ovarian Fibroma 24 0.119
558
MLG164 Malignant Epithelial Tumor of Ovary 24 0.119
559
RNL078 Renal Dysplasia 46 0.119
560
PLY100 Polyploidy 36 0.119
561
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 30 0.119
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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