Search results for "[genes] APP"

56 hits were found for '[genes] APP'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 98 25.653
2
P CRB019 Cerebral Amyloid Angiopathy 56 19.392
3
P AMY004 Amyloidosis 60 18.140
4
DMN002 Dementia 53 16.794
5
TPT001 Tauopathy 42 16.794
6
c CNT035 Central Nervous System Disease 52 15.331
7
INC002 Inclusion Body Myositis 67 13.712
8
CRB039 Cerebrovascular Disease 58 13.712
9
P MYS005 Myositis 54 13.712
10
PRN023 Prion Disease 50 13.712
11
VSC002 Vascular Dementia 47 13.712
12
P PNL007 Penile Neoplasm 34 13.712
13
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 29 13.712
14
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 27 13.712
15
c AMY091 Amyotrophic Lateral Sclerosis 1 83 11.875
16
DWN001 Down Syndrome 62 11.875
17
P DMN033 Dementia, Frontotemporal 59 11.875
18
DMN031 Dementia, Lewy Body 53 11.875
19
c ALZ037 Alzheimer Disease-2 52 11.875
20
P SPR098 Supranuclear Palsy, Progressive 52 11.875
21
P NRV007 Nervous System Disease 49 11.875
22
NRM002 Normal Pressure Hydrocephalus 49 11.875
23
ISC004 Ischemia 47 11.875
24
HMR039 Hemorrhage, Intracerebral 44 11.875
25
MNN009 Meningoencephalitis 40 11.875
26
SCR011 Scrapie 35 11.875
27
P BRN117 Bronchus Carcinoma 33 11.875
28
CRB085 Cerebral Hemorrhage 31 11.875
29
c PRK057 Parkinson Disease, Late-Onset 73 9.696
30
LSC001 Lesch-Nyhan Syndrome 64 9.696
31
c NMN015 Niemann-Pick Disease, Type C1 63 9.696
32
c INF069 Infantile Neuroaxonal Dystrophy 1 46 9.696
33
GRS011 Gerstmann-Straussler Disease 44 9.696
34
P AMY082 Amyloidosis, Familial Visceral 43 9.696
35
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 42 9.696
36
BNS003 Binswanger's Disease 40 9.696
37
PLR005 Pleuropneumonia 38 9.696
38
SYN058 Synucleinopathy 37 9.696
39
AVD001 Avoidant Personality Disorder 35 9.696
40
c ACT081 Acute Salpingitis 33 9.696
41
DSC005 Descending Colon Cancer 30 9.696
42
ATY002 Atypical Choroid Plexus Papilloma 30 9.696
43
DMN032 Dementia, Familial British 28 9.696
44
ALZ029 Alzheimer Disease Mitochondrial 25 9.696
45
c HRD084 Hereditary Cerebral Amyloid Angiopathy 25 9.696
46
P URT033 Urethra Cancer 23 9.696
47
URT032 Urethra Adenocarcinoma 20 9.696
48
ACT016 Actinobacillosis 20 9.696
49
URT024 Urethra Clear Cell Adenocarcinoma 19 9.696
50
ABT005 Abeta Amyloidosis, Dutch Type 18 9.696
51
c ALZ002 Alzheimer Disease Type 1 25 6.856
52
c L34001 L34v Amyloidosis 16 6.856
53
ABT002 Abeta Amyloidosis, Italian Type 13 6.856
54
ABT004 Abeta Amyloidosis, Iowa Type 13 6.856
55
c A21001 A21g Amyloidosis 12 6.856
56
ABT003 Abeta Amyloidosis, Arctic Type 11 6.856