Search results for "[genes] APP"

59 hits were found for '[genes] APP'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 91 23.587
2
P CRB019 Cerebral Amyloid Angiopathy 56 18.015
3
P AMY004 Amyloidosis 59 16.679
4
DMN002 Dementia 51 15.226
5
ISC004 Ischemia 49 15.226
6
INC002 Inclusion Body Myositis 63 13.618
7
P MYS005 Myositis 55 13.618
8
CRB039 Cerebrovascular Disease 55 13.618
9
VSC002 Vascular Dementia 48 13.618
10
P ANG015 Angioedema 47 13.618
11
P PNL012 Penile Cancer 44 13.618
12
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 27 13.618
13
P SCH015 Schizophrenia 76 11.794
14
c AMY091 Amyotrophic Lateral Sclerosis 1 74 11.794
15
DWN001 Down Syndrome 58 11.794
16
P DMN033 Dementia, Frontotemporal 57 11.794
17
DMN031 Dementia, Lewy Body 54 11.794
18
P SPR098 Supranuclear Palsy, Progressive 50 11.794
19
NRM002 Normal Pressure Hydrocephalus 48 11.794
20
c CNT035 Central Nervous System Disease 48 11.794
21
c ALZ037 Alzheimer Disease-2 47 11.794
22
TPT001 Tauopathy 43 11.794
23
PRN023 Prion Disease 42 11.794
24
HMR039 Hemorrhage, Intracerebral 42 11.794
25
MNN009 Meningoencephalitis 40 11.794
26
SYN058 Synucleinopathy 38 11.794
27
SCR011 Scrapie 36 11.794
28
c ALZ002 Alzheimer Disease Type 1 29 11.794
29
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 29 11.794
30
P BRN120 Bronchus Cancer 28 11.794
31
CRB085 Cerebral Hemorrhage 27 11.794
32
P PRK057 Parkinson Disease, Late-Onset 69 9.630
33
P CRT072 Creutzfeldt-Jakob Disease 60 9.630
34
c NMN015 Niemann-Pick Disease, Type C1 59 9.630
35
P NRV007 Nervous System Disease 51 9.630
36
c ALM001 Al Amyloidosis 46 9.630
37
GRS011 Gerstmann-Straussler Disease 46 9.630
38
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 44 9.630
39
P AMY082 Amyloidosis, Familial Visceral 40 9.630
40
PLR005 Pleuropneumonia 40 9.630
41
c INF069 Infantile Neuroaxonal Dystrophy 1 39 9.630
42
AVD001 Avoidant Personality Disorder 39 9.630
43
c ACT081 Acute Salpingitis 38 9.630
44
KHL003 Kohlschutter-Tonz Syndrome 33 9.630
45
DMN032 Dementia, Familial British 33 9.630
46
ATY002 Atypical Choroid Plexus Papilloma 32 9.630
47
DSC005 Descending Colon Cancer 27 9.630
48
c URT035 Urethral Benign Neoplasm 26 9.630
49
BNS003 Binswanger's Disease 25 9.630
50
URT032 Urethra Adenocarcinoma 22 9.630
51
ACT016 Actinobacillosis 21 9.630
52
URT024 Urethra Clear Cell Adenocarcinoma 18 9.630
53
c HRD084 Hereditary Cerebral Amyloid Angiopathy 16 9.630
54
ABT005 Abeta Amyloidosis, Dutch Type 16 6.809
55
ABT007 Abetal34v Amyloidosis 13 6.809
56
ABT002 Abeta Amyloidosis, Italian Type 12 6.809
57
ABT004 Abeta Amyloidosis, Iowa Type 12 6.809
58
ABT003 Abeta Amyloidosis, Arctic Type 10 6.809
59
ABT006 Abetaa21g Amyloidosis 9 6.809