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 19 15.093
2
P ALZ034 Alzheimer Disease 99 8.176
3
P CRB019 Cerebral Amyloid Angiopathy 67 6.203
4
DMN002 Dementia 65 4.386
5
INC002 Inclusion Body Myositis 80 4.268
6
P AMY004 Amyloidosis 73 4.268
7
P MYS005 Myositis 71 4.268
8
c ERL026 Early-Onset Autosomal Dominant Alzheimer Disease 35 3.670
9
BRN071 Brain Injury 57 3.445
10
MNN009 Meningoencephalitis 45 3.445
11
LKM006 Leukomalacia 31 3.445
12
NRM002 Normal Pressure Hydrocephalus 64 2.477
13
CRB085 Cerebral Hemorrhage 40 2.477
14
OCL008 Oculopharyngeal Muscular Dystrophy 64 2.436
15
P FML043 Familial Idiopathic Basal Ganglia Calcification 60 2.436
16
BSL009 Basal Ganglia Calcification 52 2.436
17
BNS003 Binswanger's Disease 52 2.436
18
P NRX001 Neuroaxonal Dystrophy 50 2.436
19
CRB090 Cerebral Hypoxia 49 2.436
20
KR002 Kuru 48 2.436
21
SYN058 Synucleinopathy 46 2.436
22
ARG005 Argyrophilic Grain Disease 44 2.436
23
CD4002 Cd40 Deficiency 41 2.436
24
PRX001 Peroxisomal Disease 38 2.436
25
CNT046 Central Nervous System Vasculitis 38 2.436
26
DMN032 Dementia, Familial British 34 2.436
27
SHK001 Shaken Baby Syndrome 34 2.436
28
c HRD084 Hereditary Cerebral Amyloid Angiopathy 33 2.436
29
c ALZ002 Alzheimer Disease Type 1 34 1.981
30
MLR004 Malaria 84 1.723
31
HRD153 Hereditary Cerebral Hemorrhage with Amyloidosis, Piedmont Type 14 1.723
32
HRD152 Hereditary Cerebral Hemorrhage with Amyloidosis, Iowa Type 13 1.723
33
HRD150 Hereditary Cerebral Hemorrhage with Amyloidosis, Italian Type 13 1.723
34
HRD151 Hereditary Cerebral Hemorrhage with Amyloidosis, Arctic Type 12 1.723
35
HRD149 Hereditary Cerebral Hemorrhage with Amyloidosis, Flemish Type 8 1.723
36
NRN002 Neuronitis 42 0.429
37
CRB009 Cerebritis 37 0.224
38
DWN001 Down Syndrome 59 0.214
39
P NRB001 Neuroblastoma 72 0.183
40
P HRP006 Herpes Simplex 66 0.112
41
P THY032 Thyroiditis 65 0.112
42
ATH003 Atherosclerosis 65 0.091
43
ISC004 Ischemia 61 0.091
44
HYP266 Hypoxia 57 0.091
45
BRN106 Burns 48 0.091
46
c HYP163 Hyperlipidemia Type 3 28 0.091
47
P OBS005 Obesity 98 0.065
48
P AST005 Asthma 91 0.065
49
P LKM002 Leukemia 76 0.065
50
P FRG001 Fragile X Syndrome 75 0.065
51
P BPL003 Bipolar Disorder 75 0.065
52
P MYL006 Myeloid Leukemia 74 0.065
53
P SDD001 Sudden Infant Death Syndrome 71 0.065
54
c PRC016 Pre-Eclampsia 67 0.065
55
P HYD006 Hydrocephalus 65 0.065
56
P HPT021 Hepatitis 63 0.065
57
P ECL001 Eclampsia 61 0.065
58
MTR014 Motor Neuron Disease 61 0.065
59
P OPN001 Open-Angle Glaucoma 59 0.065
60
GLC003 Glucose Intolerance 59 0.065
61
RHB003 Rhabdomyosarcoma 59 0.065
62
ALC006 Alcoholic Hepatitis 57 0.065
63
HPT019 Hepatic Encephalopathy 55 0.065
64
P LSS002 Lissencephaly 55 0.065
65
P BLP003 Blepharospasm 52 0.065
66
BRN080 Brain Ischemia 50 0.065
67
HMC014 Homocysteinemia 47 0.065
68
CRB004 Cerebral Artery Occlusion 42 0.065
69
APH002 Aphasia 41 0.065
70
P RNL017 Renal Oncocytoma 40 0.065
71
ORL015 Oral Squamous Cell Carcinoma 37 0.065
72
PNC041 Pancreatic Ductal Adenocarcinoma 34 0.065
73
TPT001 Tauopathy 34 0.065