Search results for VCP

135 hits were found for VCP

# Family MCID Name MIFTS Score
1
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 15.564
2
c ADL074 Adult-Onset Distal Myopathy Due to Vcp Mutation 14 7.091
3
P INC029 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1 47 5.288
4
c AMY107 Amyotrophic Lateral Sclerosis 14 with or Without Frontotemporal Dementia 26 5.262
5
P MYP004 Myopathy 70 4.629
6
P FRN006 Frontotemporal Dementia 68 4.611
7
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 4.561
8
P LTR001 Lateral Sclerosis 54 4.435
9
c AMY091 Amyotrophic Lateral Sclerosis 1 89 4.145
10
P DMN002 Dementia 66 4.076
11
P PGT001 Paget's Disease of Bone 58 3.282
12
P ALZ034 Alzheimer Disease 88 3.225
13
P CHR071 Charcot-Marie-Tooth Disease 65 3.225
14
TTH006 Tooth Disease 46 3.225
15
CYS001 Cystic Fibrosis 81 3.153
16
MLT177 Multisystem Proteinopathy 30 2.941
17
P MSC005 Muscular Dystrophy 66 2.833
18
P MTR014 Motor Neuron Disease 65 2.833
19
P MCH002 Machado-Joseph Disease 62 2.760
20
WRN001 Werner Syndrome 69 2.730
21
c HRD010 Hereditary Spastic Paraplegia 66 2.368
22
P PRK057 Parkinson Disease, Late-Onset 78 2.295
23
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 2.295
24
INC002 Inclusion Body Myositis 58 2.295
25
P MYS005 Myositis 56 2.295
26
PCK003 Pick Disease of Brain 68 2.265
27
c ATS330 Autosomal Dominant Limb-Girdle Muscular Dystrophy 32 2.265
28
P NRN021 Neuronal Ceroid Lipofuscinosis 64 2.229
29
SPC010 Speech and Communication Disorders 47 2.229
30
MMM001 Mammary Paget's Disease 53 2.166
31
c FNC030 Fanconi Anemia, Complementation Group G 41 1.761
32
P RTN008 Retinitis Pigmentosa 79 1.715
33
NRM005 Neuromuscular Disease 64 1.623
34
APH002 Aphasia 57 1.623
35
PRG033 Progressive Non-Fluent Aphasia 46 1.623
36
c PRG001 Progressive Muscular Atrophy 42 1.623
37
c INC034 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 1 22 1.623
38
c AMY074 Amyotrophic Lateral Sclerosis Type 14 21 1.623
39
SPS188 Spastic Paraplegia-Paget Disease of Bone Syndrome 20 1.623
40
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.576
41
DMN031 Dementia, Lewy Body 65 1.576
42
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 1.576
43
P BRS044 Breast Adenocarcinoma 59 1.576
44
P ZLL001 Zellweger Syndrome 57 1.576
45
PRR007 Perry Syndrome 52 1.576
46
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 51 1.576
47
P MYF003 Myofibrillar Myopathy 48 1.576
48
c AMY090 Amyotrophic Lateral Sclerosis 8 43 1.576
49
c RTN047 Retinitis Pigmentosa 18 42 1.576
50
NMN001 Nominal Aphasia 38 1.576
51
c AMY057 Amyotrophic Lateral Sclerosis 16, Juvenile 38 1.576
52
MSC190 Muscular Disease 37 1.576
53
DYS004 Dyscalculia 34 1.576
54
AGR018 Agraphia 34 1.576
55
WRT002 Writing Disorder 24 1.576
56
ASS001 Associative Agnosia 21 1.576
57
MSC004 Muscle Tissue Disease 21 1.576
58
c FNC027 Fanconi Anemia, Complementation Group a 81 0.138
59
PRP016 Paraplegia 52 0.138
60
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.112
61
P NRP001 Neuropathy 56 0.112
62
P MSC003 Muscular Atrophy 52 0.112
63
P MYS079 Miyoshi Muscular Dystrophy 50 0.112
64
RTN023 Retinitis 46 0.112
65
NRR001 Neuroretinitis 42 0.112
66
OST159 Osteogenic Sarcoma 66 0.097
67
P PRP019 Peripheral Nervous System Disease 58 0.097
68
P RTN016 Retinal Degeneration 53 0.097
69
VCC001 Vaccinia 49 0.097
70
P HPT023 Hepatocellular Carcinoma 100 0.080
71
P OVR042 Ovarian Cancer 88 0.080
72
P HNT016 Huntington Disease 72 0.080
73
P BND020 Bone Disease 59 0.080
74
P BCL017 B-Cell Lymphoma 58 0.080
75
EYD002 Eye Disease 58 0.080
76
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.080
77
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.080
78
P LNG032 Lung Cancer 98 0.056
80
IMM167 Immune Deficiency Disease 78 0.056
81
P RSP003 Respiratory Failure 74 0.056
82
P NRB001 Neuroblastoma 72 0.056
83
P WSK001 Wiskott-Aldrich Syndrome 72 0.056
84
HMN044 Human Immunodeficiency Virus Type 1 71 0.056
85
PRP027 Peripheral Vascular Disease 71 0.056
86
P MYC007 Myocardial Infarction 70 0.056
87
ADL002 Adult Syndrome 70 0.056
88
P LYM118 Lymphoma 68 0.056
89
P SYS005 Systemic Scleroderma 68 0.056
90
GST092 Gastroesophageal Reflux 67 0.056
91
c ATS007 Autism Spectrum Disorder 67 0.056
92
P CCK001 Cockayne Syndrome 66 0.056
93
P NRV007 Nervous System Disease 66 0.056
94
c SML038 Small Cell Cancer of the Lung 65 0.056
95
MNK001 Menkes Disease 64 0.056
96
c JVN010 Juvenile Rheumatoid Arthritis 64 0.056
97
GT001 Gout 64 0.056
98
MSC007 Muscle Hypertrophy 64 0.056
99
KRN002 Kearns-Sayre Syndrome 63 0.056
100
P NTR004 Neutropenia 63 0.056
101
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.056
102
ERL001 Early Myoclonic Encephalopathy 62 0.056
103
LPD008 Lipid Metabolism Disorder 62 0.056
104
P SPN046 Spinal Muscular Atrophy 62 0.056
105
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.056
106
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.056
107
P TRC086 Trichohepatoenteric Syndrome 1 62 0.056
108
TXC005 Toxic Shock Syndrome 62 0.056
109
PSR001 Psoriatic Arthritis 61 0.056
110
ACQ007 Acquired Immunodeficiency Syndrome 60 0.056
111
SQM006 Squamous Cell Carcinoma 60 0.056
112
INS001 Insulinoma 60 0.056
113
OCC006 Occipital Horn Syndrome 60 0.056
114
P PLY041 Polymyositis 57 0.056
115
P NRF002 Neurofibromatosis 56 0.056
116
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.056
117
THR013 Thoracic Outlet Syndrome 54 0.056
118
SNS003 Sensory Peripheral Neuropathy 54 0.056
119
P PTS002 Ptosis 53 0.056
120
P RTN018 Retinal Disease 53 0.056
121
DYS073 Dysphagia 50 0.056
122
TBL009 Tibial Muscular Dystrophy 50 0.056
123
P MYT002 Myotonic Dystrophy 49 0.056
124
SMN008 Semantic Dementia 47 0.056
125
NNK001 Nonaka Myopathy 46 0.056
126
P GNT009 Giant Axonal Neuropathy 45 0.056
127
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.056
128
CYT002 Cytokine Deficiency 42 0.056
129
c ERL056 Early-Onset Parkinson's Disease 39 0.056
130
WLL004 Wallerian Degeneration 39 0.056
131
FTD001 Foot Drop 33 0.056
132
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 32 0.056
133
c CRN111 Cranioectodermal Dysplasia 4 31 0.056
134
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.056
135
c ATS432 Autosomal Dominant Distal Myopathy 23 0.056
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