Search results for hnrnpa1

224 hits were found for hnrnpa1

# Family MCID Name MIFTS Score
1
c AMY063 Amyotrophic Lateral Sclerosis 20 31 36.026
2
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 31 35.740
3
c AMY091 Amyotrophic Lateral Sclerosis 1 88 28.113
4
c SCN036 Secondary Progressive Multiple Sclerosis 55 25.253
5
P LTR001 Lateral Sclerosis 58 22.602
6
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 19.592
7
P CLR023 Colorectal Cancer 100 18.862
8
P MYP004 Myopathy 67 16.379
9
RLP002 Relapsing-Remitting Multiple Sclerosis 56 16.351
10
FRN006 Frontotemporal Dementia 68 16.083
11
P DMN002 Dementia 65 14.821
12
MLT177 Multisystem Proteinopathy 30 14.679
13
P MLT020 Multiple Sclerosis 79 13.819
14
P MSC005 Muscular Dystrophy 66 13.299
15
P PGT001 Paget's Disease of Bone 60 11.185
16
P MSC003 Muscular Atrophy 52 10.867
17
P SPN046 Spinal Muscular Atrophy 62 10.842
18
IMM167 Immune Deficiency Disease 77 10.014
19
BRK010 Burkitt Lymphoma 66 9.820
20
P SPN301 Spinocerebellar Ataxia 2 59 9.820
21
OCL008 Oculopharyngeal Muscular Dystrophy 53 9.820
22
c ATS330 Autosomal Dominant Limb-Girdle Muscular Dystrophy 31 9.820
23
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 9.820
24
INF058 Inflammatory Myofibroblastic Tumor 45 7.877
25
P MTR014 Motor Neuron Disease 65 7.355
26
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 65 7.081
27
c ATR062 Atrial Septal Defect 1 39 6.944
28
DRM021 Dermatopathia Pigmentosa Reticularis 41 6.944
29
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 6.944
30
EPT024 Epithelial-Stromal Tgfbi Dystrophy 17 6.944
31
DSS008 Disease of Mental Health 74 6.944
32
END043 Endometrial Stromal Tumor 34 6.944
33
c HMN022 Human T-Cell Leukemia Virus Type 2 33 6.944
34
P LTT001 Lattice Corneal Dystrophy 30 6.944
35
END031 Endometrial Stromal Sarcoma 45 6.944
36
P PNC035 Pancreatic Cancer 86 2.009
37
P GST053 Gastric Cancer 82 1.784
38
P HPT023 Hepatocellular Carcinoma 95 1.526
39
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 33 1.504
40
P LNG064 Lung Cancer Susceptibility 3 70 1.497
41
P BRS047 Breast Cancer 97 1.455
42
P ADN016 Adenocarcinoma 63 1.386
43
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.319
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.294
45
GLM045 Glioma 62 1.241
46
GLL048 Glial Tumor 52 1.241
47
P SPP010 Suppressor of Tumorigenicity 3 51 1.224
48
P PRS040 Prostate Cancer 95 1.153
49
GST040 Gastric Adenocarcinoma 66 1.114
50
P INC035 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 3 26 1.078
51
DMY004 Demyelinating Disease 50 1.047
52
CHC001 Chickenpox 56 1.047
53
CRV035 Cervical Cancer 72 1.022
54
P LKM002 Leukemia 66 1.022
55
P MYT002 Myotonic Dystrophy 51 1.022
56
CNT061 Conotruncal Heart Malformations 66 0.965
57
DBL002 Double Outlet Right Ventricle 57 0.965
58
HRT011 Heart Septal Defect 49 0.965
59
P VNT002 Ventricular Septal Defect 58 0.965
60
P ADL010 Adult Respiratory Distress Syndrome 71 0.965
61
P ZLL001 Zellweger Syndrome 65 0.965
62
P TMR010 Tumor Predisposition Syndrome 69 0.933
63
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.933
64
CLR109 Colorectal Adenocarcinoma 50 0.933
65
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.933
66
INH023 Inherited Cancer-Predisposing Syndrome 53 0.933
67
MYL057 Myelopathy, Htlv-1-Associated 39 0.931
68
TRP002 Tropical Spastic Paraparesis 48 0.931
69
SPS019 Spastic Paraparesis 38 0.931
70
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.931
71
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.931
72
P ATX030 Ataxia-Telangiectasia 80 0.896
73
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.896
74
P OVR042 Ovarian Cancer 88 0.896
75
TLN003 Telangiectasis 51 0.896
76
HYP066 Hyperglycemia 60 0.896
77
P MYL006 Myeloid Leukemia 60 0.896
78
FTT001 Fatty Liver Disease 61 0.896
79
c LKM063 Leukemia, Chronic Myeloid 71 0.853
80
c MCR133 Microvascular Complications of Diabetes 4 41 0.853
81
MYL009 Myelodysplastic Syndrome 67 0.853
82
c MCR113 Microvascular Complications of Diabetes 3 52 0.853
83
c MCR130 Microvascular Complications of Diabetes 6 41 0.853
84
c MCR120 Microvascular Complications of Diabetes 7 47 0.853
85
c RTN041 Retinitis Pigmentosa 11 43 0.853
86
P INF038 Influenza 68 0.853
87
FBR012 Fabry Disease 71 0.659
88
P HYP061 Hypertrophic Cardiomyopathy 69 0.659
89
BRN071 Brain Injury 50 0.495
90
DGN001 Degenerative Disc Disease 48 0.455
91
c PCH010 Pachyonychia Congenita 3 43 0.363
92
P MYS005 Myositis 56 0.363
93
INC002 Inclusion Body Myositis 57 0.363
94
PRS047 Prostatitis 58 0.363
95
OST159 Osteogenic Sarcoma 66 0.363
96
NRM005 Neuromuscular Disease 63 0.363
97
STM007 Stomatitis 52 0.363
98
P LKM062 Leukemia, Acute Lymphoblastic 69 0.336
99
P PLY041 Polymyositis 59 0.336
100
P DRM010 Dermatomyositis 61 0.336
101
P SKN015 Skin Carcinoma 71 0.336
102
P LNG032 Lung Cancer 98 0.307
103
c SML038 Small Cell Cancer of the Lung 69 0.307
104
P NRB001 Neuroblastoma 66 0.307
105
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.274
106
PLY150 Polykaryocytosis Inducer 29 0.274
107
GLB002 Glioblastoma 67 0.274
108
SQM006 Squamous Cell Carcinoma 59 0.274
109
CRV038 Cervical Squamous Cell Carcinoma 56 0.274
110
P THL005 Thalassemia 56 0.274
111
CRV002 Cervix Uteri Carcinoma in Situ 48 0.274
112
CRV045 Cervical Intraepithelial Neoplasia 38 0.274
113
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.274
114
HMN044 Human Immunodeficiency Virus Type 1 76 0.238
115
ATM095 Autoimmune Disease 61 0.238
116
P BND020 Bone Disease 60 0.238
117
P KDN017 Kidney Cancer 60 0.238
118
HYP266 Hypoxia 56 0.238
119
P ALZ034 Alzheimer Disease 87 0.194
120
P BLD134 Bladder Cancer 79 0.194
121
GLC003 Glucose Intolerance 53 0.194
122
MRF001 Marfan Syndrome 76 0.194
123
MRF007 Marfanoid Hypermobility Syndrome 50 0.194
124
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.194
125
P LYM118 Lymphoma 69 0.194
126
END057 Endometrial Cancer 71 0.194
127
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.194
128
c VRL010 Viral Hepatitis 52 0.194
129
THY006 Thymus Lymphoma 27 0.194
130
LVR012 Liver Cirrhosis 62 0.194
131
c ESS001 Essential Tremor 56 0.194
132
BRN028 Brain Cancer 73 0.194
133
P LVR013 Liver Disease 68 0.194
134
SKN016 Skin Disease 62 0.194
135
CHR074 Choriocarcinoma 46 0.194
136
P LPS002 Liposarcoma 64 0.194
137
c MSC175 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 47 0.194
138
NTH001 Netherton Syndrome 60 0.194
139
MSC152 Muscular Dystrophy, Becker Type 69 0.194
140
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.194
141
GST010 Gestational Trophoblastic Neoplasm 52 0.194
142
P TRM003 Tremor 50 0.194
143
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 0.194
144
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.194
145
P RTN024 Retinoblastoma 72 0.137
146
c TYP009 Type 2 Diabetes Mellitus 92 0.137
147
VTM030 Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor 16 0.137
148
MYL069 Myeloma, Multiple 77 0.137
149
AGN016 Aging 54 0.137
150
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.137
151
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.137
152
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.137
153
CHK001 Chikungunya 60 0.137
154
ADR016 Adrenal Cortical Carcinoma 61 0.137
155
MSC007 Muscle Hypertrophy 64 0.137
156
CRB004 Cerebral Artery Occlusion 46 0.137
157
P PRK057 Parkinson Disease, Late-Onset 79 0.137
158
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.137
159
P RHM011 Rheumatoid Arthritis 81 0.137
160
UTR056 Uterine Corpus Endometrial Carcinoma 27 0.137
161
P SCL018 Scoliosis 57 0.137
162
AGR018 Agraphia 37 0.137
163
c AMY023 Amyotrophic Lateral Sclerosis Type 6 35 0.137
164
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.137
165
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.137
166
P MYC007 Myocardial Infarction 69 0.137
167
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.137
168
c SPN296 Spinocerebellar Ataxia 17 47 0.137
169
JVN004 Juvenile Myelomonocytic Leukemia 67 0.137
170
c AMY105 Amyotrophic Lateral Sclerosis 6 with or Without Frontotemporal Dementia 34 0.137
171
c HPT073 Hepatitis C Virus 71 0.137
172
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.137
173
P HNT016 Huntington Disease 73 0.137
174
c NRF024 Neurofibromatosis, Type I 76 0.137
175
FML345 Familial Expansile Osteolysis 46 0.137
176
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.137
177
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.137
178
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.137
179
c TRM017 Tremor, Hereditary Essential, 4 35 0.137
180
SHR107 Short Stature-Obesity Syndrome 25 0.137
181
EWN003 Ewing Sarcoma 70 0.137
182
P RSP003 Respiratory Failure 74 0.137
183
P GLM040 Glioma Susceptibility 1 70 0.137
184
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.137
185
MLT157 Multiple System Atrophy 1 69 0.137
186
HYP060 Hyperinsulinism 53 0.137
187
DYS004 Dyscalculia 35 0.137
188
c INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 26 0.137
189
P MYS079 Miyoshi Muscular Dystrophy 52 0.137
190
ACT098 Acute Erythroid Leukemia 55 0.137
191
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.137
192
c ACT073 Acute Leukemia 59 0.137
193
P DRR001 Diarrhea 55 0.137
194
MLG169 Malignant Astrocytoma 57 0.137
195
ISC004 Ischemia 61 0.137
196
P PRN023 Prion Disease 60 0.137
197
c HPT001 Hepatitis C 61 0.137
198
P HPT021 Hepatitis 68 0.137
199
SNS003 Sensory Peripheral Neuropathy 51 0.137
200
ALX001 Alexia 44 0.137
201
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.137
202
c DLT002 Dilated Cardiomyopathy 79 0.137
203
HMS001 Hemosiderosis 48 0.137
204
HND002 Hand, Foot and Mouth Disease 50 0.137
205
MTH009 Mouth Disease 57 0.137
206
ADR004 Adrenal Cortical Adenocarcinoma 38 0.137
207
MMM001 Mammary Paget's Disease 53 0.137
208
P THY023 Thymoma 64 0.137
209
MSC157 Muscular Dystrophy, Duchenne Type 79 0.137
210
c LKM061 Leukemia, Acute Myeloid 83 0.137
211
PHN003 Phenylketonuria 76 0.137
212
P NSP012 Nasopharyngeal Carcinoma 60 0.137
213
c THY107 Thymoma, Familial 42 0.137
214
CYT002 Cytokine Deficiency 43 0.137
215
P HRP006 Herpes Simplex 65 0.137
216
C9R003 C9orf72 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 11 0.137
217
DYS003 Dysgraphia 35 0.137
218
P ART022 Arthritis 70 0.137
219
P DBT009 Diabetes Mellitus 67 0.137
220
P NRF002 Neurofibromatosis 60 0.137
221
MCR004 Macroglobulinemia 48 0.137
222
P RRH023 Rare Hereditary Hemochromatosis 53 0.137
223
CNG506 Congenital Amyoplasia 27 0.137
224
CLS049 Classic Phenylketonuria 42 0.137
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