Search results for MAG

183 hits were found for MAG

# Family MCID Name MIFTS Score
1
c SPS213 Spastic Paraplegia 75, Autosomal Recessive 39 5.214
2
PLY113 Polyneuropathy Associated with Igm Monoclonal Gammapathy with Anti-Mag 18 4.781
3
P PLY019 Polyneuropathy 56 3.399
4
P MLT020 Multiple Sclerosis 72 2.814
5
P SCH015 Schizophrenia 74 2.769
6
P OPT009 Optic Neuritis 57 2.769
7
NRF007 Neurofibroma 64 2.743
8
KRN002 Kearns-Sayre Syndrome 63 2.743
9
P DMY001 Demyelinating Polyneuropathy 43 2.566
10
c HRD010 Hereditary Spastic Paraplegia 66 2.414
11
P CHR071 Charcot-Marie-Tooth Disease 65 2.343
12
SNS003 Sensory Peripheral Neuropathy 54 2.343
13
DMY004 Demyelinating Disease 52 2.343
14
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.321
15
NRT004 Neuritis 52 2.298
16
LYM012 Lymphoplasmacytic Lymphoma 47 2.298
17
P PLZ001 Pelizaeus-Merzbacher Disease 64 2.271
18
P LKD001 Leukodystrophy 59 2.271
19
MTR007 Motor Peripheral Neuropathy 39 2.271
20
P RTT002 Rett Syndrome 80 2.239
21
P ATS364 Autism 70 2.239
22
P MTR014 Motor Neuron Disease 65 2.239
23
P NMN002 Niemann-Pick Disease 59 2.239
24
P SBS003 Substance Abuse 55 2.239
25
CHR629 Charcot-Marie-Tooth Disease and Deafness 52 2.239
26
CNT025 Central Pontine Myelinolysis 46 2.239
27
P PRP019 Peripheral Nervous System Disease 58 2.021
28
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 1.748
29
WLL004 Wallerian Degeneration 39 1.707
30
c ATM098 Autoimmune Peripheral Neuropathy 32 1.707
31
WLD007 Waldenstroem's Macroglobulinemia 61 1.657
32
P PLY020 Polyradiculoneuropathy 48 1.657
33
c CHR094 Chronic Polyneuropathy 29 1.657
34
NRM005 Neuromuscular Disease 64 1.625
35
P GLL022 Guillain-Barre Syndrome 59 1.625
36
MNN002 Mononeuritis Multiplex 41 1.625
37
c HRD088 Hereditary Neuropathies 37 1.625
38
P MTC003 Metachromatic Leukodystrophy 70 1.584
39
c NMN013 Niemann-Pick Disease, Type a 62 1.584
40
P OPT006 Optic Nerve Disease 60 1.584
41
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 1.584
42
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 51 1.584
43
MLL002 Miller Fisher Syndrome 43 1.584
44
MNN017 Mononeuropathy 42 1.584
45
CRB001 Cerebral Lymphoma 39 1.584
46
BLD054 Blood Protein Disease 38 1.584
47
c ATM089 Autoimmune Neuropathy 34 1.584
48
c ATM007 Autoimmune Disease of Central Nervous System 28 1.584
49
c ATM105 Autoimmune Disease of Peripheral Nervous System 27 1.584
50
OST008 Osteosclerotic Myeloma 23 1.584
51
MNN016 Mononeuritis of Upper Limb and Mononeuritis Multiplex 21 1.584
52
ASY004 Asymmetric Motor Neuropathy 17 1.584
53
P NRP001 Neuropathy 56 0.486
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.217
55
P TRM003 Tremor 54 0.187
56
MCR004 Macroglobulinemia 49 0.150
57
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.141
58
c PRM038 Primary Agammaglobulinemia 44 0.112
59
P NRV007 Nervous System Disease 66 0.100
60
TTH006 Tooth Disease 46 0.100
61
ALL014 Allergic Encephalomyelitis 38 0.100
62
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.100
63
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.086
64
P NRB001 Neuroblastoma 72 0.086
65
HMN044 Human Immunodeficiency Virus Type 1 71 0.086
66
CRB039 Cerebrovascular Disease 67 0.086
67
P GLM045 Glioma 63 0.086
68
ATM095 Autoimmune Disease 62 0.086
69
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.086
70
P LTR001 Lateral Sclerosis 54 0.086
71
PRP016 Paraplegia 52 0.086
72
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.086
73
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.086
74
PLS009 Plasma Cell Neoplasm 51 0.086
75
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.086
76
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.086
77
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.086
78
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.086
79
GLL048 Glial Tumor 45 0.086
80
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.086
81
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.086
82
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.086
83
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.086
84
CYT002 Cytokine Deficiency 42 0.086
85
P AXN001 Axonal Neuropathy 36 0.086
86
CYS001 Cystic Fibrosis 81 0.071
87
STR067 Stroke, Ischemic 81 0.071
88
P LKM071 Leukemia, Chronic Lymphocytic 79 0.071
89
P AMY004 Amyloidosis 70 0.071
90
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.071
91
LVR012 Liver Cirrhosis 62 0.071
92
c PNS012 Paine Syndrome 61 0.071
93
SPN186 Spinal Cord Injury 60 0.071
94
P BCL017 B-Cell Lymphoma 58 0.071
95
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.071
96
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.071
97
CRB004 Cerebral Artery Occlusion 45 0.071
98
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.071
99
ATX019 Ataxia with Vitamin E Deficiency 42 0.071
100
PRS063 Paresthesia 41 0.071
101
c LKM005 Leukemia, T-Cell, Chronic 34 0.071
102
P PRS040 Prostate Cancer 97 0.050
103
P BRS047 Breast Cancer 97 0.050
104
P OVR042 Ovarian Cancer 88 0.050
105
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.050
106
P RTN008 Retinitis Pigmentosa 79 0.050
107
IMM167 Immune Deficiency Disease 78 0.050
108
P PRK057 Parkinson Disease, Late-Onset 78 0.050
109
ULC004 Ulcerative Colitis 73 0.050
110
P CNR004 Cone-Rod Dystrophy 2 73 0.050
111
ANX010 Anxiety 73 0.050
112
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.050
113
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.050
114
PRP027 Peripheral Vascular Disease 71 0.050
115
P MYC007 Myocardial Infarction 70 0.050
116
DWN001 Down Syndrome 70 0.050
117
ADL002 Adult Syndrome 70 0.050
118
CRB037 Cerebral Palsy 69 0.050
119
LYM133 Lymphoma, Hodgkin, Classic 69 0.050
120
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.050
121
P TRN020 Turner Syndrome 67 0.050
122
ALC007 Alcohol Dependence 66 0.050
123
P PRS038 Personality Disorder 65 0.050
124
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.050
125
MSC007 Muscle Hypertrophy 64 0.050
126
P VSC007 Vascular Disease 63 0.050
127
P CRN300 Coronary Heart Disease 1 63 0.050
128
CLT003 Colitis 62 0.050
129
LPP008 Lipoprotein Quantitative Trait Locus 62 0.050
130
P TRC086 Trichohepatoenteric Syndrome 1 62 0.050
131
P VSC011 Vasculitis 62 0.050
132
DPH001 Diphtheria 60 0.050
133
ACQ007 Acquired Immunodeficiency Syndrome 60 0.050
134
SPP011 Suppression of Tumorigenicity 12 59 0.050
135
P SLP005 Sleep Disorder 59 0.050
136
P LYM033 Lymphoproliferative Syndrome 59 0.050
137
P CYS018 Cystitis 59 0.050
138
ERY029 Erythermalgia, Primary 58 0.050
139
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.050
140
CNS004 Constipation 58 0.050
141
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.050
142
THR024 Thrombosis 57 0.050
143
CYT008 Cytomegalovirus Infection 57 0.050
144
ALL006 Allergic Asthma 56 0.050
145
ERY051 Erythroleukemia, Familial 56 0.050
146
BCT022 Bacterial Infectious Disease 56 0.050
147
P DRR001 Diarrhea 55 0.050
148
P SLM003 Salmonellosis 55 0.050
149
THR013 Thoracic Outlet Syndrome 54 0.050
150
PRP080 Peripheral Artery Disease 53 0.050
151
P RTN018 Retinal Disease 53 0.050
152
ART140 Arteries, Anomalies of 52 0.050
153
PTH003 Pathologic Nystagmus 52 0.050
154
APR001 Apraxia 52 0.050
155
P MNN019 Mannosidosis, Beta a, Lysosomal 51 0.050
156
BHR001 Behr Syndrome 51 0.050
157
MNN009 Meningoencephalitis 49 0.050
158
PTH002 Pathological Gambling 49 0.050
159
QDR001 Quadriplegia 48 0.050
160
CRY004 Cryoglobulinemia 48 0.050
161
P RNV001 Renovascular Hypertension 48 0.050
162
HLX001 Helix Syndrome 47 0.050
163
CRD137 Cardiogenic Shock 47 0.050
164
RTN023 Retinitis 46 0.050
165
MLT075 Multifocal Motor Neuropathy 46 0.050
166
P CHR345 Chronic Pain 44 0.050
167
CVD001 Covid-19 44 0.050
168
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 43 0.050
169
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.050
170
BCK006 Back Pain 42 0.050
171
NRR001 Neuroretinitis 42 0.050
172
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.050
173
c PST041 Posterior Urethral Valves 41 0.050
174
c GLL037 Guillain-Barre Syndrome, Familial 39 0.050
175
P DYS021 Dysautonomia 39 0.050
176
c HRD223 Hereditary Melanoma 39 0.050
177
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
178
OCL015 Oculomotor Apraxia 37 0.050
179
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 23 0.050
180
c RDC016 Reducing Body Myopathy, X-Linked 1a, Severe, with Infantile or Early Childhood Onset 22 0.050
181
P RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 22 0.050
182
P CMP101 Complex Hereditary Spastic Paraplegia 20 0.050
183
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.050
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