Search results for "APP"

80 hits were found for 'APP'
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# Family MCID Name MIFTS Score
1
P ALZ001 Alzheimer's Disease 100 8.855
2
c ALZ003 Alzheimer Disease Type 2 68 6.315
3
c ALZ011 Alzheimer Disease 1, Familial 17 6.315
4
c ALZ009 Alzheimer Disease Type 5 21 6.101
5
c ALZ017 Alzheimer Disease-10 19 6.101
6
c ALZ015 Alzheimer Disease 6 18 6.101
7
c ALZ016 Alzheimer Disease 8 18 6.101
8
c ALZ028 Alzheimer Disease 9, Late Onset 18 6.101
9
ALZ024 Alzheimer Disease, Pathogenesis, Association with 18 6.101
10
P CRB019 Cerebral Amyloid Angiopathy 64 5.000
11
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 4.337
12
DMN002 Dementia 67 4.155
13
INC002 Inclusion Body Myositis 86 4.041
14
P MYS005 Myositis 70 4.041
15
P AMY004 Amyloidosis 68 4.041
16
LWY001 Lewy Body Dementia 63 3.261
17
BRN071 Brain Injury 58 3.261
18
MNN009 Meningoencephalitis 47 3.261
19
LKM006 Leukomalacia 33 3.261
20
NRM002 Normal Pressure Hydrocephalus 62 2.345
21
HRD042 Hereditary Cerebral Hemorrhage with Amyloidosis 43 2.345
22
CRB085 Cerebral Hemorrhage 39 2.345
23
OCL008 Oculopharyngeal Muscular Dystrophy 64 2.306
24
P FML043 Familial Idiopathic Basal Ganglia Calcification 61 2.306
25
BNS003 Binswanger's Disease 53 2.306
26
P PRM052 Primary Progressive Aphasia 52 2.306
27
CRB090 Cerebral Hypoxia 49 2.306
28
NRX001 Neuroaxonal Dystrophy 49 2.306
29
CD4002 Cd40 Deficiency 47 2.306
30
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 47 2.306
31
KR002 Kuru 47 2.306
32
SYN058 Synucleinopathy 46 2.306
33
ARG005 Argyrophilic Grain Disease 44 2.306
34
c NRX003 Neuroaxonal Dystrophy, Infantile 39 2.306
35
CNT046 Central Nervous System Vasculitis 39 2.306
36
PRX001 Peroxisomal Disease 39 2.306
37
SHK001 Shaken Baby Syndrome 34 2.306
38
c HRD084 Hereditary Cerebral Amyloid Angiopathy 34 2.306
39
c MNS008 Monosomy 21 32 2.306
40
c ALZ002 Alzheimer Disease Type 1 35 1.631
41
AMN007 Aminoacylase 1 Deficiency 28 1.631
42
NRN002 Neuronitis 44 0.417
43
DWN001 Down Syndrome 62 0.215
44
CRB009 Cerebritis 39 0.215
45
P NRB001 Neuroblastoma 70 0.164
46
P HRP006 Herpes Simplex 68 0.108
47
c THY032 Thyroiditis 66 0.108
48
ATH003 Atherosclerosis 69 0.088
49
ISC004 Ischemia 63 0.088
50
HYP266 Hypoxia 58 0.088
51
MMR004 Memory Impairment 51 0.088
52
BRN106 Burns 50 0.088
53
P HYP163 Hyperlipidemia Type 3 28 0.088
54
P PRK002 Parkinson's Disease 93 0.062
55
P OBS005 Obesity 91 0.062
56
P AST005 Asthma 89 0.062
57
P FML021 Familial Hypercholesterolemia 86 0.062
58
P MLT020 Multiple Sclerosis 85 0.062
59
P LKM002 Leukemia 77 0.062
60
P FRG001 Fragile X Syndrome 76 0.062
61
c MYL006 Myeloid Leukemia 75 0.062
62
c HYP095 Hypercholesterolemia 73 0.062
63
P SDD001 Sudden Infant Death Syndrome 71 0.062
64
P FRN006 Frontotemporal Dementia 70 0.062
65
P HYD006 Hydrocephalus 68 0.062
66
c HPT021 Hepatitis 64 0.062
67
MTR014 Motor Neuron Disease 62 0.062
68
GLC003 Glucose Intolerance 62 0.062
69
c OPN001 Open-Angle Glaucoma 60 0.062
70
RHB003 Rhabdomyosarcoma 59 0.062
71
c LSS002 Lissencephaly 57 0.062
72
HPT019 Hepatic Encephalopathy 57 0.062
73
c PRM010 Primary Open Angle Glaucoma 55 0.062
74
BRN080 Brain Ischemia 51 0.062
75
HMC014 Homocysteinemia 49 0.062
76
P BLP003 Blepharospasm 48 0.062
77
c APH002 Aphasia 44 0.062
78
CRB004 Cerebral Artery Occlusion 44 0.062
79
ORL015 Oral Squamous Cell Carcinoma 38 0.062
80
TPT001 Tauopathy 35 0.062