Search results for "[genes] APP"

36 hits were found for '[genes] APP'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 100 32.352
2
P CRB019 Cerebral Amyloid Angiopathy 59 25.060
3
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 15 22.876
4
INC002 Inclusion Body Myositis 71 17.720
5
P AMY004 Amyloidosis 63 17.720
6
P MYS005 Myositis 63 17.720
7
DMN002 Dementia 58 17.720
8
BRN071 Brain Injury 49 14.468
9
MNN009 Meningoencephalitis 39 14.468
10
c ERL026 Early-Onset Autosomal Dominant Alzheimer Disease 31 14.468
11
LKM006 Leukomalacia 27 14.468
12
OCL008 Oculopharyngeal Muscular Dystrophy 56 10.231
13
NRM002 Normal Pressure Hydrocephalus 56 10.231
14
P FML043 Familial Idiopathic Basal Ganglia Calcification 52 10.231
15
BSL009 Basal Ganglia Calcification 46 10.231
16
BNS003 Binswanger's Disease 44 10.231
17
P NRX001 Neuroaxonal Dystrophy 43 10.231
18
CRB090 Cerebral Hypoxia 43 10.231
19
KR002 Kuru 42 10.231
20
SYN058 Synucleinopathy 39 10.231
21
ARG005 Argyrophilic Grain Disease 38 10.231
22
CD4002 Cd40 Deficiency 35 10.231
23
CRB085 Cerebral Hemorrhage 35 10.231
24
PRX001 Peroxisomal Disease 33 10.231
25
CNT046 Central Nervous System Vasculitis 32 10.231
26
DMN032 Dementia, Familial British 30 10.231
27
SHK001 Shaken Baby Syndrome 29 10.231
28
c HRD084 Hereditary Cerebral Amyloid Angiopathy 28 10.231
29
MLR004 Malaria 81 7.234
30
c ALZ037 Alzheimer Disease-2 45 7.234
31
c ALZ002 Alzheimer Disease Type 1 29 7.234
32
HRD153 Hereditary Cerebral Hemorrhage with Amyloidosis, Piedmont Type 12 7.234
33
HRD152 Hereditary Cerebral Hemorrhage with Amyloidosis, Iowa Type 12 7.234
34
HRD150 Hereditary Cerebral Hemorrhage with Amyloidosis, Italian Type 12 7.234
35
HRD151 Hereditary Cerebral Hemorrhage with Amyloidosis, Arctic Type 10 7.234
36
HRD149 Hereditary Cerebral Hemorrhage with Amyloidosis, Flemish Type 7 7.234