Search results for MAPT

193 hits were found for MAPT

# Family MCID Name MIFTS Score
1
P FRN006 Frontotemporal Dementia 68 5.166
2
P PRK057 Parkinson Disease, Late-Onset 78 4.070
3
P ALZ034 Alzheimer Disease 88 3.870
4
P SPR120 Supranuclear Palsy, Progressive, 1 68 3.849
5
P DMN002 Dementia 66 3.717
6
PCK003 Pick Disease of Brain 68 3.627
7
PRK087 Parkinson-Dementia Syndrome 33 3.435
8
APR001 Apraxia 52 2.582
9
P SYN057 Syndromic Intellectual Disability 41 2.571
10
CRT072 Creutzfeldt-Jakob Disease 70 2.477
11
APH002 Aphasia 57 2.370
12
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.346
13
P MTR014 Motor Neuron Disease 65 2.249
14
SMN008 Semantic Dementia 47 2.214
15
CRT033 Corticobasal Degeneration 57 2.206
16
P HNT016 Huntington Disease 72 2.151
17
P AMY004 Amyloidosis 70 2.151
18
INC002 Inclusion Body Myositis 58 2.151
19
VSC002 Vascular Dementia 57 2.151
20
P MYS005 Myositis 56 2.151
21
P EPL164 Epilepsy 71 2.125
22
DWN001 Down Syndrome 70 2.125
23
P HYD006 Hydrocephalus 66 2.125
25
P BPL003 Bipolar Disorder 56 2.125
26
P NRM002 Normal Pressure Hydrocephalus 54 2.125
27
SCR011 Scrapie 39 2.125
28
MLT157 Multiple System Atrophy 1 70 1.873
29
P TRM003 Tremor 54 1.873
30
P MVM001 Movement Disease 63 1.836
31
P KLN006 Koolen-De Vries Syndrome 49 1.836
32
P RSP003 Respiratory Failure 74 1.815
33
P NRB001 Neuroblastoma 72 1.815
34
c ESS001 Essential Tremor 56 1.792
35
DMN031 Dementia, Lewy Body 65 1.766
36
P SLP005 Sleep Disorder 59 1.766
37
c ALZ049 Alzheimer Disease 2 49 1.766
38
LRN003 Learning Disability 49 1.766
39
SPC010 Speech and Communication Disorders 47 1.766
40
AGR018 Agraphia 34 1.766
41
STR067 Stroke, Ischemic 81 1.735
42
P SCH015 Schizophrenia 74 1.735
43
P ATS364 Autism 70 1.735
44
P MYP004 Myopathy 70 1.735
45
CRB039 Cerebrovascular Disease 67 1.735
46
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 1.735
47
TRN015 Transient Cerebral Ischemia 63 1.735
48
P SPN046 Spinal Muscular Atrophy 62 1.735
49
P PRN023 Prion Disease 57 1.735
50
P RST001 Restless Legs Syndrome 54 1.735
51
FCL014 Focal Epilepsy 54 1.735
52
c CNT035 Central Nervous System Disease 52 1.735
53
DMY004 Demyelinating Disease 52 1.735
54
NRT004 Neuritis 52 1.735
55
P OLV001 Olivopontocerebellar Atrophy 51 1.735
56
P MTC133 Mitochondrial Myopathy 49 1.735
57
WRN003 Wernicke Encephalopathy 47 1.735
58
PST027 Postencephalitic Parkinson Disease 46 1.735
59
BSL009 Basal Ganglia Calcification 41 1.735
60
c PRK090 Parkinson Disease 3, Autosomal Dominant 40 1.735
62
AMN003 Amnestic Disorder 54 1.324
63
KHL003 Kohlschutter-Tonz Syndrome 65 1.298
64
PRG033 Progressive Non-Fluent Aphasia 46 1.298
65
MTS001 Mutism 46 1.298
66
RMS001 Rem Sleep Behavior Disorder 46 1.298
67
SPC005 Speech Disorder 43 1.298
68
CLS047 Classic Progressive Supranuclear Palsy Syndrome 31 1.298
69
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 1.267
70
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 1.267
71
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 1.267
72
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 51 1.267
73
P MCR364 Macrodactyly 40 1.267
74
NMN001 Nominal Aphasia 38 1.267
75
c ALZ057 Alzheimer Disease 10 37 1.267
76
PST086 Posterior Cortical Atrophy 37 1.267
77
DYS003 Dysgraphia 36 1.267
78
IDM001 Ideomotor Apraxia 32 1.267
79
PRG116 Progressive Supranuclear Palsy-Corticobasal Syndrome 24 1.267
80
PRG117 Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome 15 1.267
81
PRG115 Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome 15 1.267
82
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 1.227
83
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 1.227
84
DSS008 Disease of Mental Health 58 1.227
85
GRS011 Gerstmann-Straussler Disease 56 1.227
87
PLV003 Pelvic Inflammatory Disease 55 1.227
88
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 54 1.227
89
TXC002 Toxic Encephalopathy 53 1.227
90
PRR007 Perry Syndrome 52 1.227
91
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 1.227
92
FTL002 Fatal Familial Insomnia 49 1.227
93
NRN008 Neuronal Intranuclear Inclusion Disease 46 1.227
94
P CMM008 Communicating Hydrocephalus 45 1.227
95
ANR009 Aneurysmal Bone Cysts 43 1.227
96
c ALZ045 Alzheimer Disease 9 43 1.227
97
BNS003 Binswanger's Disease 42 1.227
99
CRB033 Cerebral Degeneration 42 1.227
100
PCD001 Pica Disease 41 1.227
101
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 41 1.227
102
ALX001 Alexia 39 1.227
103
AKN002 Akinetic Mutism 37 1.227
104
ART010 Arteriolosclerosis 37 1.227
105
GRS001 Gerstmann Syndrome 36 1.227
106
ECH002 Echolalia 34 1.227
107
VSL003 Visual Agnosia 34 1.227
108
P PRS013 Prosopagnosia 33 1.227
109
CHR362 Chromosome 17q21.31 Duplication Syndrome 32 1.227
110
P MYX008 Myxoid Chondrosarcoma 32 1.227
111
ALZ029 Alzheimer Disease Mitochondrial 32 1.227
112
c PST018 Posterior Cerebral Artery Infarction 31 1.227
113
SPC003 Specific Developmental Disorder 31 1.227
114
P CHR084 Chromosomal Disease 30 1.227
115
SML010 Simultanagnosia 30 1.227
116
c ALZ060 Alzheimer Disease 14 29 1.227
117
TMP002 Temporal Lobe Neoplasm 27 1.227
118
CRB211 Cerebral Cortical Dysplasia 25 1.227
119
PLY179 Polyomavirus-Associated Nephropathy 24 1.227
120
WRT002 Writing Disorder 24 1.227
121
PRL006 Paralytic Lagophthalmos 21 1.227
122
ASS001 Associative Agnosia 21 1.227
123
FNG001 Finger Agnosia 20 1.227
124
c SPN444 Spinal Muscular Atrophy Type 0 17 1.227
125
RRG004 Rare Genetic Syndromic Intellectual Disability 15 0.482
126
P LTR001 Lateral Sclerosis 54 0.182
127
P PRS040 Prostate Cancer 97 0.129
128
P MYC033 Myoclonus 46 0.084
129
GRN059 Grn Frontotemporal Dementia 14 0.084
130
P LNG032 Lung Cancer 98 0.069
131
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.069
132
DPR016 Depression 63 0.069
133
MNT002 Mental Depression 58 0.069
134
TRM010 Traumatic Brain Injury 51 0.069
135
HDN002 Head Injury 46 0.069
136
c PRK093 Parkinson Disease 8, Autosomal Dominant 44 0.069
137
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.069
138
P RRN010 Rare Neurodegenerative Disease 20 0.069
139
P GST053 Gastric Cancer 83 0.049
140
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.049
141
BRN028 Brain Cancer 74 0.049
142
ANX010 Anxiety 73 0.049
143
P MLT020 Multiple Sclerosis 72 0.049
144
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.049
145
P ANG001 Angelman Syndrome 69 0.049
146
P MYS003 Myasthenia Gravis 68 0.049
147
RCK004 Rickets 68 0.049
148
P MJR001 Major Depressive Disorder 68 0.049
149
P TRN020 Turner Syndrome 67 0.049
150
c ATS007 Autism Spectrum Disorder 67 0.049
151
c SML038 Small Cell Cancer of the Lung 65 0.049
152
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.049
153
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.049
154
P ERL057 Early Infantile Epileptic Encephalopathy 63 0.049
155
P GLM045 Glioma 63 0.049
156
P PLY014 Polycystic Kidney Disease 62 0.049
157
ATM095 Autoimmune Disease 62 0.049
158
MDD011 Mood Disorder 62 0.049
159
NTR005 Nutritional Deficiency Disease 62 0.049
160
P ENC018 Encephalopathy 61 0.049
161
P SCL018 Scoliosis 60 0.049
162
P OPT006 Optic Nerve Disease 60 0.049
163
PST028 Post-Traumatic Stress Disorder 58 0.049
164
P ALC033 Alcohol Use Disorder 58 0.049
165
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.049
166
P NRP001 Neuropathy 56 0.049
167
AGN016 Aging 56 0.049
168
P LNG035 Lung Large Cell Carcinoma 54 0.049
169
CLR030 Clear Cell Renal Cell Carcinoma 53 0.049
170
HMC014 Homocysteinemia 53 0.049
171
P PNC025 Panic Disorder 53 0.049
172
P OVR082 Overgrowth Syndrome 50 0.049
173
DYS073 Dysphagia 50 0.049
174
BRN071 Brain Injury 49 0.049
175
ACT084 Acute Stress Disorder 47 0.049
176
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.049
177
GLL048 Glial Tumor 45 0.049
178
c PRK052 Parkinson Disease 17 43 0.049
179
ANT019 Anterograde Amnesia 38 0.049
180
ALL014 Allergic Encephalomyelitis 38 0.049
181
P CRB088 Cerebral Atrophy 37 0.049
182
P HRD217 Hereditary Optic Neuropathy 36 0.049
183
MNT302 Mental Retardation, X-Linked, Syndromic, Christianson Type 35 0.049
184
c PRK025 Parkinson Disease 10 33 0.049
185
PLY150 Polykaryocytosis Inducer 31 0.049
186
MLT116 Multiple System Atrophy, Parkinsonian Type 30 0.049
187
c PRK099 Parkinson Disease 18, Autosomal Dominant 24 0.049
188
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.049
190
c PRK058 Parkinson Disease 16 17 0.049
191
ALN006 Alien Hand Syndrome 16 0.049
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