Search results for "APP"

79 hits were found for 'APP'
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# Family MCID Name MIFTS Score
1
P ALZ001 Alzheimer's Disease 98 8.905
2
c ALZ003 Alzheimer Disease Type 2 69 6.352
3
c ALZ011 Alzheimer Disease 1, Familial 17 6.352
4
c ALZ009 Alzheimer Disease Type 5 22 6.137
5
c ALZ017 Alzheimer Disease-10 21 6.137
6
c ALZ015 Alzheimer Disease 6 18 6.137
7
c ALZ016 Alzheimer Disease 8 18 6.137
8
c ALZ028 Alzheimer Disease 9, Late Onset 18 6.137
9
ALZ024 Alzheimer Disease, Pathogenesis, Association with 17 6.137
10
P CRB019 Cerebral Amyloid Angiopathy 64 5.029
11
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 31 4.362
12
DMN002 Dementia 66 4.179
13
INC002 Inclusion Body Myositis 86 4.065
14
P AMY004 Amyloidosis 73 4.065
15
P MYS005 Myositis 71 4.065
16
LWY001 Lewy Body Dementia 64 3.280
17
BRN071 Brain Injury 57 3.280
18
MNN009 Meningoencephalitis 46 3.280
19
LKM006 Leukomalacia 32 3.280
20
NRM002 Normal Pressure Hydrocephalus 65 2.359
21
HRD042 Hereditary Cerebral Hemorrhage with Amyloidosis 43 2.359
22
CRB085 Cerebral Hemorrhage 40 2.359
23
OCL008 Oculopharyngeal Muscular Dystrophy 64 2.320
24
P FML043 Familial Idiopathic Basal Ganglia Calcification 62 2.320
25
BNS003 Binswanger's Disease 52 2.320
26
P PRM052 Primary Progressive Aphasia 51 2.320
27
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 50 2.320
28
CD4002 Cd40 Deficiency 49 2.320
29
CRB090 Cerebral Hypoxia 49 2.320
30
NRX001 Neuroaxonal Dystrophy 48 2.320
31
KR002 Kuru 48 2.320
32
SYN058 Synucleinopathy 46 2.320
33
ARG005 Argyrophilic Grain Disease 43 2.320
34
c NRX003 Neuroaxonal Dystrophy, Infantile 39 2.320
35
CNT046 Central Nervous System Vasculitis 38 2.320
36
PRX001 Peroxisomal Disease 38 2.320
37
SHK001 Shaken Baby Syndrome 34 2.320
38
c HRD084 Hereditary Cerebral Amyloid Angiopathy 33 2.320
39
c MNS008 Monosomy 21 31 2.320
40
c ALZ002 Alzheimer Disease Type 1 34 1.640
41
NRN002 Neuronitis 43 0.418
42
DWN001 Down Syndrome 61 0.216
43
CRB009 Cerebritis 38 0.216
44
P NRB001 Neuroblastoma 70 0.165
45
P HRP006 Herpes Simplex 66 0.108
46
c THY032 Thyroiditis 65 0.108
47
ATH003 Atherosclerosis 68 0.088
48
ISC004 Ischemia 62 0.088
49
HYP266 Hypoxia 57 0.088
50
MMR004 Memory Impairment 50 0.088
51
BRN106 Burns 49 0.088
52
P HYP163 Hyperlipidemia Type 3 29 0.088
53
P PRK002 Parkinson's Disease 92 0.062
54
P OBS005 Obesity 89 0.062
55
P AST005 Asthma 87 0.062
56
P FML021 Familial Hypercholesterolemia 85 0.062
57
P MLT020 Multiple Sclerosis 84 0.062
58
P FRG001 Fragile X Syndrome 77 0.062
59
P LKM002 Leukemia 76 0.062
60
c MYL006 Myeloid Leukemia 74 0.062
61
P FRN006 Frontotemporal Dementia 72 0.062
62
c HYP095 Hypercholesterolemia 72 0.062
63
P SDD001 Sudden Infant Death Syndrome 71 0.062
64
P HYD006 Hydrocephalus 69 0.062
65
c HPT021 Hepatitis 63 0.062
66
MTR014 Motor Neuron Disease 61 0.062
67
GLC003 Glucose Intolerance 61 0.062
68
c OPN001 Open-Angle Glaucoma 59 0.062
69
RHB003 Rhabdomyosarcoma 58 0.062
70
c LSS002 Lissencephaly 56 0.062
71
HPT019 Hepatic Encephalopathy 56 0.062
72
c PRM010 Primary Open Angle Glaucoma 54 0.062
73
BRN080 Brain Ischemia 50 0.062
74
HMC014 Homocysteinemia 48 0.062
75
P BLP003 Blepharospasm 47 0.062
76
c APH002 Aphasia 43 0.062
77
CRB004 Cerebral Artery Occlusion 43 0.062
78
ORL015 Oral Squamous Cell Carcinoma 38 0.062
79
TPT001 Tauopathy 35 0.062