Search results for "APP"

77 hits were found for 'APP'
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# Family MCID Name MIFTS Score
1
P ALZ001 Alzheimer's Disease 97 7.937
2
c ALZ003 Alzheimer Disease Type 2 67 6.204
3
c ALZ011 Alzheimer Disease 1, Familial 10 6.204
4
c ALZ009 Alzheimer Disease Type 5 14 5.978
5
ALZ024 Alzheimer Disease, Pathogenesis, Association with 14 5.978
6
c ALZ015 Alzheimer Disease 6 12 5.978
7
c ALZ017 Alzheimer Disease-10 12 5.978
8
c ALZ016 Alzheimer Disease 8 11 5.978
9
c ALZ028 Alzheimer Disease 9, Late Onset 11 5.978
10
DMN002 Dementia 66 4.223
11
P CRB019 Cerebral Amyloid Angiopathy 60 4.188
12
INC002 Inclusion Body Myositis 77 4.109
13
P AMY004 Amyloidosis 67 4.109
14
MYS005 Myositis 66 4.109
15
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 4.086
16
LWY001 Lewy Body Dementia 61 3.316
17
BRN071 Brain Injury 57 3.316
18
MNN009 Meningoencephalitis 46 3.316
19
LKM006 Leukomalacia 33 3.316
20
NRM002 Normal Pressure Hydrocephalus 61 2.385
21
HRD042 Hereditary Cerebral Hemorrhage with Amyloidosis 43 2.385
22
P AMY001 Amyotrophic Lateral Sclerosis 98 2.345
23
OCL008 Oculopharyngeal Muscular Dystrophy 63 2.345
24
P PRM052 Primary Progressive Aphasia 55 2.345
25
BNS003 Binswanger's Disease 52 2.345
26
NRX001 Neuroaxonal Dystrophy 49 2.345
27
CRB090 Cerebral Hypoxia 48 2.345
28
CD4002 Cd40 Deficiency 47 2.345
29
c FML043 Familial Idiopathic Basal Ganglia Calcification 46 2.345
30
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 46 2.345
31
ARG005 Argyrophilic Grain Disease 43 2.345
32
KR002 Kuru 43 2.345
33
CNT046 Central Nervous System Vasculitis 38 2.345
34
PRX001 Peroxisomal Disease 37 2.345
35
c NRX003 Neuroaxonal Dystrophy, Infantile 36 2.345
36
SHK001 Shaken Baby Syndrome 34 2.345
37
c HRD084 Hereditary Cerebral Amyloid Angiopathy 32 2.345
38
c MNS008 Monosomy 21 31 2.345
39
NRN002 Neuronitis 43 0.420
40
DWN001 Down Syndrome 61 0.217
41
CRB009 Cerebritis 39 0.217
42
P NRB001 Neuroblastoma 70 0.166
43
P HRP006 Herpes Simplex 66 0.108
44
c THY032 Thyroiditis 66 0.108
45
ATH003 Atherosclerosis 68 0.089
46
ISC004 Ischemia 63 0.089
47
HYP266 Hypoxia 57 0.089
48
MMR004 Memory Impairment 50 0.089
49
P HYP163 Hyperlipidemia Type 3 27 0.089
50
P PRK002 Parkinson's Disease 92 0.063
51
P OBS005 Obesity 89 0.063
52
P AST005 Asthma 88 0.063
53
P FML021 Familial Hypercholesterolemia 85 0.063
54
P LKM002 Leukemia 77 0.063
55
P FRG001 Fragile X Syndrome 73 0.063
56
c MYL006 Myeloid Leukemia 72 0.063
57
c HYP095 Hypercholesterolemia 70 0.063
58
P FRN006 Frontotemporal Dementia 70 0.063
59
P MLT020 Multiple Sclerosis 69 0.063
60
P HYD006 Hydrocephalus 68 0.063
61
c HPT021 Hepatitis 64 0.063
62
MTR014 Motor Neuron Disease 61 0.063
63
P GLC007 Glaucoma 60 0.063
64
GLC003 Glucose Intolerance 58 0.063
65
c OPN001 Open-Angle Glaucoma 57 0.063
66
RHB003 Rhabdomyosarcoma 57 0.063
67
c LSS002 Lissencephaly 56 0.063
68
HPT019 Hepatic Encephalopathy 55 0.063
69
c PRM010 Primary Open Angle Glaucoma 55 0.063
70
ENC006 Encephalomyelitis 52 0.063
71
BRN080 Brain Ischemia 50 0.063
72
BRN106 Burns 49 0.063
73
HMC014 Homocysteinemia 48 0.063
74
c APH002 Aphasia 44 0.063
75
CRB004 Cerebral Artery Occlusion 43 0.063
76
ORL015 Oral Squamous Cell Carcinoma 36 0.063
77
TPT001 Tauopathy 35 0.063