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Search results for grb2

466 hits were found for grb2

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 21.095
2
P CLR023 Colorectal Cancer 100 19.430
3
P LNG032 Lung Cancer 98 18.943
4
P HPT023 Hepatocellular Carcinoma 95 18.377
5
P PRS040 Prostate Cancer 95 18.255
6
c HPT001 Hepatitis C 61 17.590
7
P GST053 Gastric Cancer 82 17.572
8
P WSK001 Wiskott-Aldrich Syndrome 72 15.241
9
P HPT021 Hepatitis 68 15.114
10
P PHC003 Pheochromocytoma 70 14.903
11
c LKM063 Leukemia, Chronic Myeloid 70 14.049
12
PNC129 Pancreatic Adenocarcinoma 64 13.003
13
c HPT073 Hepatitis C Virus 70 11.820
14
c HPT007 Hepatitis E 50 10.687
15
PFF001 Pfeiffer Syndrome 77 10.521
16
P CNR004 Cone-Rod Dystrophy 2 74 10.521
17
P PLC011 Pilocytic Astrocytoma 55 10.521
18
RSP023 Rasopathy 54 8.395
19
NNN026 Noonan Syndrome with Multiple Lentigines 64 7.772
20
P CRD224 Cardiofaciocutaneous Syndrome 1 71 7.557
21
P SKN009 Skin Granular Cell Tumor 31 7.439
22
P MYL006 Myeloid Leukemia 60 3.010
23
P LKM002 Leukemia 65 2.871
24
INS024 Insulin-Like Growth Factor I 77 2.400
25
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.080
26
ADR040 Adrenal Gland Pheochromocytoma 45 2.018
27
c LKM061 Leukemia, Acute Myeloid 83 1.948
28
P PNC035 Pancreatic Cancer 87 1.925
29
c SML038 Small Cell Cancer of the Lung 68 1.899
30
ADL002 Adult Syndrome 69 1.865
31
END057 Endometrial Cancer 76 1.865
32
FLL027 Fallopian Tube Carcinoma 66 1.865
33
P OVR042 Ovarian Cancer 88 1.845
34
P LNG064 Lung Cancer Susceptibility 3 69 1.817
35
PRT037 Pertussis 49 1.778
36
P NRB001 Neuroblastoma 66 1.686
37
HLX001 Helix Syndrome 47 1.617
38
MYL009 Myelodysplastic Syndrome 67 1.605
39
P ADN016 Adenocarcinoma 63 1.544
40
MYL069 Myeloma, Multiple 76 1.532
41
CYT002 Cytokine Deficiency 43 1.493
42
P MLN008 Melanoma 75 1.465
43
ACT098 Acute Erythroid Leukemia 55 1.411
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.400
45
SQM006 Squamous Cell Carcinoma 59 1.364
46
SVR004 Severe Combined Immunodeficiency 70 1.352
47
P ALZ034 Alzheimer Disease 87 1.333
48
P MLT074 Multiple Endocrine Neoplasia 58 1.299
49
P HRP006 Herpes Simplex 65 1.285
50
P HNT016 Huntington Disease 73 1.271
51
THY029 Thyroid Carcinoma 55 1.256
52
P LYM118 Lymphoma 66 1.208
53
P ANP001 Anaplastic Large Cell Lymphoma 59 1.208
54
P SCH015 Schizophrenia 74 1.190
55
HYP266 Hypoxia 56 1.172
56
HYP066 Hyperglycemia 60 1.154
57
VCC001 Vaccinia 49 1.130
58
c SYS001 Systemic Lupus Erythematosus 85 1.088
59
P LPS004 Lupus Erythematosus 61 1.088
60
P NNN008 Noonan Syndrome 1 76 1.079
61
c PSD047 Pseudo-Turner Syndrome 52 1.079
62
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.078
63
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.063
64
OST159 Osteogenic Sarcoma 66 1.063
65
GLB002 Glioblastoma 67 1.051
66
c CHR064 Chronic Monocytic Leukemia 35 1.029
67
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.029
68
P NSP012 Nasopharyngeal Carcinoma 60 1.021
69
SRC027 Sarcoma, Synovial 58 1.004
70
P LKM062 Leukemia, Acute Lymphoblastic 69 0.990
71
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.956
72
P BLD134 Bladder Cancer 79 0.956
73
P LYM033 Lymphoproliferative Syndrome 59 0.956
74
ALL014 Allergic Encephalomyelitis 34 0.956
75
P SKN015 Skin Carcinoma 71 0.938
76
P BCL017 B-Cell Lymphoma 57 0.938
77
GLM045 Glioma 62 0.938
78
GLL048 Glial Tumor 51 0.938
79
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.919
80
BNR002 Bone Resorption Disease 47 0.919
81
STR067 Stroke, Ischemic 79 0.898
82
c MCR115 Microvascular Complications of Diabetes 5 65 0.898
83
P OST001 Osteopetrosis 70 0.898
84
ISC004 Ischemia 61 0.898
85
P HYP098 Hypereosinophilic Syndrome 66 0.898
86
PRT251 Proteinuria, Chronic Benign 58 0.877
87
c SCH079 Schizophrenia 1 44 0.877
88
c BRN108 Branchiootic Syndrome 1 63 0.877
89
P LSS002 Lissencephaly 52 0.877
90
c LSS005 Lissencephaly 1 57 0.877
91
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.877
92
ESP021 Esophageal Cancer 84 0.877
93
MGC001 Megacolon 48 0.877
94
P LTR001 Lateral Sclerosis 57 0.877
95
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.877
96
47X002 47,xyy 47 0.877
97
c MJR022 Major Affective Disorder 8 37 0.854
98
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.854
99
P MDL005 Medulloblastoma 75 0.854
100
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.854
101
c MJR024 Major Affective Disorder 9 40 0.854
102
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.854
103
c NRF023 Neurofibromatosis, Type Ii 70 0.854
104
DFF005 Diffuse Large B-Cell Lymphoma 55 0.854
105
MCS002 Mucositis 55 0.854
106
MYL031 Myeloproliferative Neoplasm 66 0.854
107
P BPL003 Bipolar Disorder 56 0.854
108
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.854
109
c PRC016 Pre-Eclampsia 64 0.854
110
P NRF002 Neurofibromatosis 60 0.854
111
FTT001 Fatty Liver Disease 61 0.854
112
P MSC005 Muscular Dystrophy 66 0.854
113
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.829
114
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.829
115
P MYC007 Myocardial Infarction 69 0.829
116
THY111 Thyroid Carcinoma, Familial Medullary 67 0.829
117
P SPN301 Spinocerebellar Ataxia 2 59 0.829
118
CMB007 Combined Immunodeficiency 56 0.829
119
P HMN010 Hemangioma 61 0.829
120
THY125 Thyroid Gland Medullary Carcinoma 48 0.829
121
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.829
122
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.829
123
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.801
124
PLY150 Polykaryocytosis Inducer 29 0.801
125
P HRS035 Hirschsprung Disease 1 66 0.801
126
EWN003 Ewing Sarcoma 69 0.801
127
c PCH010 Pachyonychia Congenita 3 43 0.801
128
CHL065 Cholangiocarcinoma 57 0.801
129
P LKM071 Leukemia, Chronic Lymphocytic 74 0.801
130
P GLM040 Glioma Susceptibility 1 70 0.801
131
MLG169 Malignant Astrocytoma 57 0.801
132
SPN035 Spindle Cell Sarcoma 51 0.801
133
P GST044 Gastritis 55 0.801
134
INT079 Intrahepatic Cholangiocarcinoma 51 0.801
135
SRC014 Sarcoma 64 0.801
136
P SLV027 Silver-Russell Syndrome 1 52 0.800
137
DNC004 Diencephalic Syndrome 36 0.800
138
SPP011 Suppression of Tumorigenicity 12 61 0.769
139
BRK010 Burkitt Lymphoma 65 0.769
140
HMN047 Human Cytomegalovirus Infection 59 0.769
141
MST004 Mast Cell Neoplasm 41 0.769
142
P PRP019 Peripheral Nervous System Disease 57 0.769
143
c HPT016 Hepatitis B 62 0.769
144
P ATR005 Atrophic Gastritis 50 0.769
145
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.769
146
c LKM005 Leukemia, T-Cell, Chronic 33 0.769
147
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.732
148
c FBR084 Fibromatosis, Gingival, 1 51 0.732
149
c DFN376 Deafness, Autosomal Recessive 114 16 0.732
150
c ATS006 Autosomal Recessive Nonsyndromic Deafness 36 0.732
151
ATS010 Autosomal Recessive Disease 42 0.732
152
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.732
153
P GNG025 Gingival Fibromatosis 48 0.732
154
P SNS001 Sensorineural Hearing Loss 60 0.732
155
P LRY044 Larynx Cancer 53 0.732
156
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.732
157
GNG013 Gingivitis 59 0.732
158
GNG011 Gingival Disease 53 0.732
159
GST040 Gastric Adenocarcinoma 66 0.732
160
DBT010 Diabetic Neuropathy 54 0.732
161
P NRP001 Neuropathy 59 0.732
162
c NNS007 Nonsyndromic Deafness 36 0.732
163
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.732
164
FBR019 Fibromatosis 44 0.732
165
WRN001 Werner Syndrome 69 0.683
166
P MYC084 Mycobacterium Tuberculosis 1 68 0.683
167
P MLN069 Melanoma, Uveal 59 0.683
168
HLC007 Helicobacter Pylori Infection 67 0.683
169
EXT050 Extraneural Perineurioma 16 0.683
170
LWG006 Low Grade Glioma 41 0.683
171
P FLL037 Follicular Lymphoma 66 0.683
172
P ART021 Arteriosclerosis 53 0.683
173
BRS099 Breast Ductal Carcinoma 61 0.683
174
ART008 Arteriosclerosis Obliterans 40 0.683
175
PRN022 Perineurioma 36 0.683
176
P RHB003 Rhabdomyosarcoma 66 0.683
177
EXT007 Extracutaneous Mastocytoma 38 0.683
178
P MYC008 Myocarditis 59 0.683
179
SFT003 Soft Tissue Sarcoma 43 0.683
180
CHR020 Chronic Interstitial Cystitis 36 0.599
181
SPL004 Splenic Marginal Zone Lymphoma 50 0.566
182
LYM133 Lymphoma, Hodgkin, Classic 69 0.566
183
LMB062 Limb Ischemia 55 0.566
184
MRG003 Marginal Zone B-Cell Lymphoma 52 0.566
185
NWC001 Newcastle Disease 47 0.566
186
CLL014 Cll/sll 45 0.566
187
LYM019 Lymphosarcoma 46 0.566
188
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 41 0.566
189
PRM163 Primary Mediastinal Large B-Cell Lymphoma 40 0.566
190
DWN001 Down Syndrome 70 0.390
191
NRL016 Neural Tube Defects 80 0.346
192
P RNL017 Renal Oncocytoma 54 0.346
193
CHR177 Chromophobe Renal Cell Carcinoma 54 0.346
194
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.346
195
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.333
196
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.333
197
CRV035 Cervical Cancer 72 0.311
198
c ACT073 Acute Leukemia 59 0.288
199
P PLY018 Polycythemia 56 0.288
200
ATM095 Autoimmune Disease 61 0.263
201
GST023 Gastric Ulcer 52 0.263
202
P PLY011 Polycystic Ovary Syndrome 57 0.263
203
MCR013 Microphthalmia 59 0.263
204
OVR094 Ovarian Epithelial Cancer 39 0.263
205
P RTN024 Retinoblastoma 72 0.235
206
CRZ001 Crouzon Syndrome 64 0.235
207
DNH001 Donohue Syndrome 60 0.235
208
LPP008 Lipoprotein Quantitative Trait Locus 65 0.235
209
LMY014 Leiomyoma, Uterine 55 0.235
210
P PRK057 Parkinson Disease, Late-Onset 79 0.235
211
HYP748 Hypertelorism 46 0.235
212
LNT004 Lentigines 45 0.235
213
CLN003 Clonorchiasis 42 0.235
214
HGH043 High Grade Glioma 46 0.235
215
ALL029 Allergic Disease 61 0.235
216
LMY002 Leiomyoma 51 0.235
217
SKN016 Skin Disease 63 0.235
218
APR006 Apert Syndrome 69 0.204
219
ART140 Arteries, Anomalies of 52 0.204
220
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.204
221
P MLT020 Multiple Sclerosis 79 0.204
222
P DRM053 Dermatitis, Atopic 65 0.204
223
HMC014 Homocysteinemia 52 0.204
224
c CHL119 Cholangitis, Primary Sclerosing 57 0.204
225
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.204
226
GST019 Gastrointestinal Stromal Tumor 78 0.204
227
MTC018 Metachondromatosis 48 0.204
228
P LPR012 Leopard Syndrome 1 48 0.204
229
c THR071 Thrombocytopenia 1 48 0.204
230
FRY006 Fryns Microphthalmia Syndrome 52 0.204
231
HYP060 Hyperinsulinism 53 0.204
232
P CRN037 Craniosynostosis 67 0.204
233
P FBR017 Fibrosarcoma 55 0.204
234
P SCL009 Sclerosing Cholangitis 46 0.204
235
ESP025 Esophagus Adenocarcinoma 37 0.204
236
PRM236 Primary Biliary Cholangitis 62 0.204
237
P THR014 Thrombocytopenia 66 0.204
238
CRB004 Cerebral Artery Occlusion 45 0.204
239
P CHL066 Cholangitis 51 0.204
240
ORL011 Oral Cancer 60 0.204
241
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 0.204
242
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.204
243
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.166
244
ORL015 Oral Squamous Cell Carcinoma 43 0.166
245
P INF037 Inflammatory Bowel Disease 53 0.166
246
P RHM011 Rheumatoid Arthritis 81 0.166
247
ATH013 Atherosclerosis Susceptibility 63 0.166
248
c NRF024 Neurofibromatosis, Type I 76 0.166
249
c TYP009 Type 2 Diabetes Mellitus 91 0.166
250
c ERY058 Erythrocytosis, Familial, 1 55 0.166
251
ERY051 Erythroleukemia, Familial 37 0.166
252
c SCL052 Scleroderma, Familial Progressive 60 0.166
253
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.166
254
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.166
255
c PRD040 Periodontitis, Chronic 52 0.166
256
MSC007 Muscle Hypertrophy 64 0.166
257
PLY001 Polycythemia Vera 69 0.166
258
c THY107 Thymoma, Familial 42 0.166
259
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.166
260
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.166
261
P AST005 Asthma 75 0.166
262
MNN043 Meningioma, Familial 79 0.166
263
JVN004 Juvenile Myelomonocytic Leukemia 66 0.166
264
HMN044 Human Immunodeficiency Virus Type 1 76 0.166
265
CHL123 Chlamydia 58 0.166
266
P THY023 Thymoma 64 0.166
267
CHL147 Chlamydia Pneumonia 47 0.166
268
P ECL001 Eclampsia 52 0.166
269
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.166
270
CKT002 Cakut 48 0.166
271
c VRL010 Viral Hepatitis 52 0.166
272
P END044 Endometriosis 62 0.166
273
SCR001 Secretory Meningioma 40 0.166
274
P LVR013 Liver Disease 68 0.166
275
MTH009 Mouth Disease 57 0.166
276
P PTT006 Pituitary Adenoma 55 0.166
277
P BRS044 Breast Adenocarcinoma 58 0.166
278
INT395 Intracranial Meningioma 47 0.166
279
P AGG001 Aggressive Periodontitis 55 0.166
280
CHL004 Cholelithiasis 48 0.166
281
P ART022 Arthritis 70 0.166
282
SCR011 Scrapie 39 0.166
283
P RTN018 Retinal Disease 53 0.166
284
P PRN023 Prion Disease 60 0.166
285
THL004 Theileriasis 26 0.166
286
BLR013 Biliary Tract Cancer 43 0.166
287
VRL011 Viral Infectious Disease 60 0.166
288
P ENC004 Encephalitis 61 0.166
289
P PRD008 Periodontitis 63 0.166
290
RTC005 Reticulosarcoma 47 0.166
291
MSL001 Measles 61 0.166
292
CRH001 Crohn's Disease 80 0.166
293
48X005 48,xyyy 39 0.166
294
HRP009 Herpes Simplex Encephalitis 58 0.166
295
PRN029 Parainfluenza Virus Type 3 32 0.166
296
CHR178 Chromosomal Triplication 33 0.166
298
P 8P1002 8p11 Myeloproliferative Syndrome 35 0.166
299
NNT018 Neonatal Herpes 23 0.166
300
CLT003 Colitis 63 0.118
301
c NNN010 Noonan Syndrome 3 51 0.118
302
c MLT086 Multiple Endocrine Neoplasia, Type Iv 51 0.118
303
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.118
304
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.118
305
DFC004 Deficiency Anemia 74 0.118
306
BRN032 Brain Glioma 45 0.118
307
P CRN038 Carney Complex Variant 63 0.118
308
c FNC029 Fanconi Anemia, Complementation Group I 55 0.118
309
P APL001 Aplastic Anemia 72 0.118
310
c DFN168 Deafness, Autosomal Recessive 26 26 0.118
311
DFN363 Deafness, Autosomal Recessive 26, Modifier of 15 0.118
312
P MTR004 Maturity-Onset Diabetes of the Young 66 0.118
313
c HGH033 High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 1 9 0.118
314
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.118
315
ING001 Inguinal Hernia 59 0.118
316
FBR054 Fibroma 44 0.118
317
DCT002 Ductal Carcinoma in Situ 58 0.118
318
END020 Endocardial Fibroelastosis 53 0.118
319
WLL001 Williams-Beuren Syndrome 60 0.118
320
P OST002 Osteoporosis 76 0.118
321
PRX015 Paroxysmal Extreme Pain Disorder 56 0.118
322
P PLV020 Pelvic Organ Prolapse 57 0.118
323
P PRD006 Prader-Willi Syndrome 60 0.118
324
c GLC092 Glaucoma, Primary Open Angle 60 0.118
325
ALC007 Alcohol Dependence 65 0.118
326
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.118
327
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.118
328
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.118
329
P MCR129 Microvascular Complications of Diabetes 1 67 0.118
330
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.118
331
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.118
332
NTR036 Neutropenia, Severe Congenital, X-Linked 35 0.118
333
AGM019 Agammaglobulinemia, X-Linked 71 0.118
334
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.118
335
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.118
336
IMM196 Immunodeficiency 15a 20 0.118
337
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.118
338
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.118
339
c MCR112 Microvascular Complications of Diabetes 2 42 0.118
340
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.118
341
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.118
342
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.118
343
ABT001 Abetalipoproteinemia 68 0.118
344
P CHN012 Chondrosarcoma 56 0.118
345
CST001 Costello Syndrome 68 0.118
346
KPS004 Kaposi Sarcoma 76 0.118
347
c HMC039 Hemochromatosis, Type 1 73 0.118
348
PRG014 Progesterone Resistance 42 0.118
349
P RTN008 Retinitis Pigmentosa 79 0.118
350
P SJG008 Sjogren Syndrome 60 0.118
351
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.118
352
MCR183 Microcephaly-Capillary Malformation Syndrome 34 0.118
353
P MMB011 Membranous Nephropathy 50 0.118
355
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.118
356
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.118
357
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.118
358
P ANG001 Angelman Syndrome 64 0.118
359
c EXS019 Exostoses, Multiple, Type I 54 0.118
360
c MST023 Mesothelioma, Malignant 56 0.118
361
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 0.118
362
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.118
363
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.118
364
c XRD032 Xeroderma Pigmentosum, Complementation Group B 50 0.118
365
c RTN046 Retinitis Pigmentosa 17 37 0.118
366
P ADL017 Adult T-Cell Leukemia 53 0.118
367
P SPL061 Split Hand-Foot Malformation 43 0.118
368
DPH001 Diphtheria 59 0.118
369
PRP036 Peripheral T-Cell Lymphoma 52 0.118
370
P DDN001 Duodenal Ulcer 52 0.118
371
NRL005 Neurilemmoma 60 0.118
372
P CNT005 Central Nervous System Lymphoma 51 0.118
373
P TCD001 Tic Disorder 50 0.118
374
ERY007 Erythropoietin Polycythemia 14 0.118
375
ACR007 Acromegaly 70 0.118
376
PPL022 Papilloma 53 0.118
377
P BNG032 Benign Mesothelioma 53 0.118
378
P BNG095 Benign Giant Cell Tumor 43 0.118
379
P VSC007 Vascular Disease 62 0.118
380
P BNC003 Bone Cancer 58 0.118
381
c MLG084 Malignant Fibrous Histiocytoma 62 0.118
382
P LMY004 Leiomyosarcoma 62 0.118
383
HMS001 Hemosiderosis 48 0.118
384
P SPN046 Spinal Muscular Atrophy 62 0.118
385
P DRR001 Diarrhea 55 0.118
386
ANG046 Angioimmunoblastic T-Cell Lymphoma 50 0.118
387
P CHR285 Chronic Myelomonocytic Leukemia 59 0.118
388
END011 Endometriosis of Ovary 40 0.118
389
BRN004 Brain Edema 54 0.118
390
P CRV031 Cervical Adenocarcinoma 48 0.118
391
c ADL052 Adult Acute Lymphocytic Leukemia 46 0.118
392
c INF023 Inflammatory Breast Carcinoma 48 0.118
393
ADN018 Adenoma 58 0.118
394
ANL017 Anal Squamous Cell Carcinoma 44 0.118
395
GST045 Gastroenteritis 58 0.118
396
IRN002 Iron Metabolism Disease 56 0.118
397
NDL024 Nodal Marginal Zone Lymphoma 36 0.118
398
STT001 Status Epilepticus 58 0.118
399
NRR001 Neuroretinitis 42 0.118
400
SQM002 Squamous Cell Papilloma 45 0.118
401
P GLM007 Glomerulonephritis 59 0.118
402
P AGM001 Agammaglobulinemia 67 0.118
403
P KDN017 Kidney Cancer 60 0.118
404
DRM006 Dermatitis 61 0.118
405
P RHN004 Rhinitis 56 0.118
406
P SYS005 Systemic Scleroderma 73 0.118
407
MYF001 Myofibroma 42 0.118
408
PST011 Pustulosis of Palm and Sole 52 0.118
409
INS001 Insulinoma 59 0.118
410
P PLM036 Pulmonary Fibrosis 65 0.118
411
LNG039 Lung Squamous Cell Carcinoma 57 0.118
412
ESN005 Eosinophilic Gastroenteritis 55 0.118
413
HMT002 Hematologic Cancer 61 0.118
414
BRN005 Brain Glioblastoma Multiforme 34 0.118
415
P ART023 Arthropathy 59 0.118
416
P TRT010 Teratoma 50 0.118
417
P GRV001 Graves' Disease 54 0.118
418
HYP043 Hyperandrogenism 47 0.118
419
P OPN001 Open-Angle Glaucoma 55 0.118
420
CHR073 Choreatic Disease 53 0.118
421
c PRM012 Primary Polycythemia 58 0.118
422
ACS001 Acoustic Neuroma 55 0.118
423
NPH113 Nephroma 37 0.118
424
DDN003 Duodenum Adenocarcinoma 37 0.118
425
P HML001 Hemolytic-Uremic Syndrome 52 0.118
426
P DMN002 Dementia 65 0.118
427
HYD002 Hydronephrosis 58 0.118
428
GT001 Gout 63 0.118
429
P HML002 Hemolytic Anemia 62 0.118
430
RTN023 Retinitis 45 0.118
431
HPT022 Hepatoblastoma 54 0.118
432
P MST002 Mast-Cell Leukemia 50 0.118
433
ALL006 Allergic Asthma 55 0.118
434
P FBR003 Fibrous Histiocytoma 43 0.118
435
LRN003 Learning Disability 49 0.118
436
BRN056 Bronchopulmonary Dysplasia 57 0.118
437
P PSR002 Psoriasis 63 0.118
438
BBS001 Babesiosis 48 0.118
439
CWP001 Cowpox 44 0.118
440
ULC004 Ulcerative Colitis 74 0.118
441
PPT005 Peptic Ulcer Disease 58 0.118
442
P MSC003 Muscular Atrophy 52 0.118
443
c CNG023 Congenital Fibrosarcoma 42 0.118
444
CHL045 Choline Deficiency Disease 39 0.118
445
OST012 Osteoarthritis 77 0.118
446
P RTN016 Retinal Degeneration 52 0.118
447
P INF038 Influenza 68 0.118
448
STM007 Stomatitis 52 0.118
449
P INS002 in Situ Carcinoma 52 0.118
450
P THL005 Thalassemia 56 0.118
451
PTT037 Pituitary Tumors 44 0.118
452
PRM243 Primary Bone Cancer 22 0.118
453
PRM226 Primary Central Nervous System Lymphoma 47 0.118
454
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.118
455
CMP097 Complex Chromosomal Rearrangement 23 0.118
456
ANX004 Anoxia 40 0.118
457
FML168 Familial Isolated Pituitary Adenoma 33 0.118
458
SYS071 Systemic Autoimmune Disease 35 0.118
459
P RRH023 Rare Hereditary Hemochromatosis 52 0.118
460
NNT021 Neonatal Meningitis 22 0.118
461
SPL018 Splenomegaly 47 0.118
462
c HRD088 Hereditary Neuropathies 34 0.118
463
HRD112 Hereditary Thrombocytopenia with Normal Platelets 24 0.118
464
c ACT134 Acute Liver Failure 57 0.118
465
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 42 0.118
466
P OVR082 Overgrowth Syndrome 41 0.118
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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