Search results for "APP"

73 hits were found for 'APP'

# Family MCID Name MIFTS Score
1
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 15 15.047
2
P ALZ034 Alzheimer Disease 100 8.136
3
P CRB019 Cerebral Amyloid Angiopathy 59 6.166
4
DMN002 Dementia 58 4.360
5
INC002 Inclusion Body Myositis 71 4.242
6
P AMY004 Amyloidosis 63 4.242
7
P MYS005 Myositis 63 4.242
8
c ERL026 Early-Onset Autosomal Dominant Alzheimer Disease 31 3.649
9
BRN071 Brain Injury 49 3.423
10
MNN009 Meningoencephalitis 39 3.423
11
LKM006 Leukomalacia 27 3.423
12
NRM002 Normal Pressure Hydrocephalus 56 2.462
13
CRB085 Cerebral Hemorrhage 35 2.462
14
OCL008 Oculopharyngeal Muscular Dystrophy 56 2.421
15
P FML043 Familial Idiopathic Basal Ganglia Calcification 52 2.421
16
BSL009 Basal Ganglia Calcification 46 2.421
17
BNS003 Binswanger's Disease 44 2.421
18
P NRX001 Neuroaxonal Dystrophy 43 2.421
19
CRB090 Cerebral Hypoxia 43 2.421
20
KR002 Kuru 42 2.421
21
SYN058 Synucleinopathy 39 2.421
22
ARG005 Argyrophilic Grain Disease 38 2.421
23
CD4002 Cd40 Deficiency 35 2.421
24
PRX001 Peroxisomal Disease 33 2.421
25
CNT046 Central Nervous System Vasculitis 32 2.421
26
DMN032 Dementia, Familial British 30 2.421
27
SHK001 Shaken Baby Syndrome 29 2.421
28
c HRD084 Hereditary Cerebral Amyloid Angiopathy 28 2.421
29
c ALZ037 Alzheimer Disease-2 45 2.011
30
c ALZ002 Alzheimer Disease Type 1 29 1.970
31
MLR004 Malaria 81 1.712
32
HRD153 Hereditary Cerebral Hemorrhage with Amyloidosis, Piedmont Type 12 1.712
33
HRD152 Hereditary Cerebral Hemorrhage with Amyloidosis, Iowa Type 12 1.712
34
HRD150 Hereditary Cerebral Hemorrhage with Amyloidosis, Italian Type 12 1.712
35
HRD151 Hereditary Cerebral Hemorrhage with Amyloidosis, Arctic Type 10 1.712
36
HRD149 Hereditary Cerebral Hemorrhage with Amyloidosis, Flemish Type 7 1.712
37
NRN002 Neuronitis 36 0.429
38
CRB009 Cerebritis 33 0.224
39
DWN001 Down Syndrome 51 0.215
40
P NRB001 Neuroblastoma 68 0.183
41
P HRP006 Herpes Simplex 63 0.112
42
P THY032 Thyroiditis 56 0.112
43
ATH003 Atherosclerosis 56 0.091
44
ISC004 Ischemia 53 0.091
45
HYP266 Hypoxia 49 0.091
46
BRN106 Burns 42 0.091
47
c HYP163 Hyperlipidemia Type 3 23 0.091
48
P OBS005 Obesity 94 0.065
49
P AST005 Asthma 84 0.065
50
P LKM002 Leukemia 66 0.065
51
P FRG001 Fragile X Syndrome 66 0.065
52
P BPL003 Bipolar Disorder 65 0.065
53
P MYL006 Myeloid Leukemia 64 0.065
54
P SDD001 Sudden Infant Death Syndrome 62 0.065
55
c PRC016 Pre-Eclampsia 58 0.065
56
P HYD006 Hydrocephalus 56 0.065
57
P HPT021 Hepatitis 55 0.065
58
P ECL001 Eclampsia 53 0.065
59
MTR014 Motor Neuron Disease 53 0.065
60
P OPN001 Open-Angle Glaucoma 51 0.065
61
GLC003 Glucose Intolerance 50 0.065
62
RHB003 Rhabdomyosarcoma 49 0.065
63
P LSS002 Lissencephaly 47 0.065
64
HPT019 Hepatic Encephalopathy 51 0.065
65
P BLP003 Blepharospasm 45 0.065
66
BRN080 Brain Ischemia 43 0.065
67
HMC014 Homocysteinemia 40 0.065
68
CRB004 Cerebral Artery Occlusion 36 0.065
69
APH002 Aphasia 35 0.065
70
P RNL017 Renal Oncocytoma 43 0.065
71
ORL015 Oral Squamous Cell Carcinoma 33 0.065
72
PNC041 Pancreatic Ductal Adenocarcinoma 38 0.065
73
TPT001 Tauopathy 29 0.065