166 hits were found for 'APP'
Try searching for appl

# ++ Fam MCID Name MIFTS Score
1
P ALZ001 Alzheimer's Disease 93 4.939
2
NRN002 Neuronitis 47 3.676
3
CRB009 Cerebritis 46 3.676
4
P DMN002 Dementia 61 2.978
5
CRB019 Cerebral Amyloid Angiopathy 60 2.950
6
INC002 Inclusion Body Myositis 66 2.886
7
P AMY004 Amyloidosis 65 2.886
8
MYS005 Myositis 61 2.886
9
LWY001 Lewy Body Dementia 60 2.847
10
c ALZ011 Alzheimer Disease 1, Familial 6 2.847
11
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 25 2.621
12
P PRK002 Parkinson's Disease 86 2.349
13
APH002 Aphasia 49 2.349
14
AMY012 Amyloidosis Cerebral 22 2.349
15
PCK001 Pick's Disease 68 2.325
16
P PRN023 Prion Disease 60 2.325
17
c PNC044 Pancreatitis 58 2.325
18
BRN071 Brain Injury 57 2.325
19
OCL008 Oculopharyngeal Muscular Dystrophy 55 2.325
20
PRV004 Periventricular Leukomalacia 54 2.325
21
MNN009 Meningoencephalitis 49 2.325
22
c ALM001 Al Amyloidosis 49 2.325
23
PRM052 Primary Progressive Aphasia 48 2.325
24
LKM006 Leukomalacia 45 2.325
25
BNS003 Binswanger's Disease 42 2.325
26
CD4002 Cd40 Deficiency 40 2.325
27
PRX001 Peroxisomal Disease 40 2.325
28
ARG005 Argyrophilic Grain Disease 36 2.325
29
HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 29 2.325
30
HRD042 Hereditary Cerebral Hemorrhage with Amyloidosis 29 2.325
31
CNT046 Central Nervous System Vasculitis 28 2.325
32
HRD084 Hereditary Cerebral Amyloid Angiopathy 28 2.325
33
ALZ008 Alzheimer Disease Risk Factor 23 2.325
34
c MNS008 Monosomy 21 22 2.325
35
HYP266 Hypoxia 60 2.064
36
ISC004 Ischemia 57 2.064
37
P MLT020 Multiple Sclerosis 75 2.040
38
P FRN006 Frontotemporal Dementia 66 2.040
39
DWN001 Down Syndrome 58 2.040
40
BRN080 Brain Ischemia 52 2.040
41
P AMY001 Amyotrophic Lateral Sclerosis 87 2.013
42
P HNT001 Huntington's Disease 81 2.013
43
P MLT019 Multiple Myeloma 76 2.013
44
P AST007 Astrocytoma 70 2.013
45
c ENC004 Encephalitis 56 2.013
46
c MYL007 Myeloma 53 2.013
47
CRB039 Cerebrovascular Disease 53 2.013
48
c LTR001 Lateral Sclerosis 52 2.013
49
c MYP004 Myopathy 52 2.013
50
TPT001 Tauopathy 50 2.013
51
TRT001 Teratocarcinoma 40 2.013
52
BRN029 Brain Disease 60 1.974
53
P NRB001 Neuroblastoma 60 1.804
54
P HRP006 Herpes Simplex 57 1.727
55
ATH003 Atherosclerosis 69 1.703
56
MMR004 Memory Impairment 52 1.703
57
P OBS005 Obesity 79 1.676
58
P NMN002 Niemann-Pick Disease 72 1.676
59
LKM002 Leukemia 70 1.676
60
c HYP095 Hypercholesterolemia 65 1.676
61
MYL006 Myeloid Leukemia 64 1.676
62
P HYD006 Hydrocephalus 60 1.676
63
SQM006 Squamous Cell Carcinoma 58 1.676
64
NRM002 Normal Pressure Hydrocephalus 54 1.676
65
ENC006 Encephalomyelitis 49 1.676
66
ORL015 Oral Squamous Cell Carcinoma 40 1.676
67
P NRF002 Neurofibromatosis 86 1.644
68
P PNC035 Pancreatic Cancer 82 1.644
69
CDS001 Cadasil 80 1.644
70
P HYP075 Hypertension 76 1.644
71
WLS001 Wilson Disease 74 1.644
72
P TYP020 Type 1 Diabetes 73 1.644
73
PHC003 Pheochromocytoma 71 1.644
74
AGR001 Age Related Macular Degeneration 71 1.644
75
P SCH015 Schizophrenia 69 1.644
76
c DBT009 Diabetes Mellitus 68 1.644
77
P CLR023 Colorectal Cancer 66 1.644
78
P MLR004 Malaria 66 1.644
79
c HPT021 Hepatitis 65 1.644
80
VSC011 Vasculitis 65 1.644
81
ART021 Arteriosclerosis 63 1.644
82
c HPT016 Hepatitis B 62 1.644
83
P INS005 Insulin Resistance 62 1.644
84
c MNN013 Meningitis 62 1.644
85
LNG032 Lung Cancer 61 1.644
86
c THY032 Thyroiditis 61 1.644
87
TTN003 Tetanus 60 1.644
88
P CRN157 Coronary Heart Disease 59 1.644
89
HDC001 Headache 58 1.644
90
CRB021 Cerebral Malaria 58 1.644
91
P PRD008 Periodontitis 58 1.644
92
c HRD002 Hereditary Angioedema 58 1.644
93
c ATX004 Ataxia 56 1.644
94
c NRN021 Neuronal Ceroid Lipofuscinosis 56 1.644
95
P MLN008 Melanoma 56 1.644
96
CHL014 Cholera 56 1.644
97
P CNJ013 Conjunctivitis 55 1.644
98
HYP037 Hyperhomocysteinemia 55 1.644
99
VSC002 Vascular Dementia 55 1.644
100
c MCP010 Mucopolysaccharidosis 55 1.644
101
TRM010 Traumatic Brain Injury 54 1.644
102
P PLY019 Polyneuropathy 54 1.644
103
c MSC005 Muscular Dystrophy 54 1.644
104
P ANG015 Angioedema 54 1.644
105
RTN023 Retinitis 53 1.644
106
RHM027 Rheumatic Disease 52 1.644
107
CHR008 Choroiditis 51 1.644
108
c MNT147 Mental Retardation 51 1.644
109
END072 Endotheliitis 51 1.644
110
PRS047 Prostatitis 50 1.644
111
OBS001 Obstructive Jaundice 50 1.644
112
HDN002 Head Injury 49 1.644
113
NRX001 Neuroaxonal Dystrophy 46 1.644
114
TXC002 Toxic Encephalopathy 45 1.644
115
CRB090 Cerebral Hypoxia 45 1.644
116
P MYF003 Myofibrillar Myopathy 43 1.644
117
P AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 41 1.644
118
c RTN016 Retinal Degeneration 41 1.644
119
c NRX003 Neuroaxonal Dystrophy, Infantile 39 1.644
120
P FML043 Familial Idiopathic Basal Ganglia Calcification 38 1.644
121
NSP002 Nasopharyngitis 38 1.644
122
SCR011 Scrapie 37 1.644
123
DFF012 Differentiating Neuroblastoma 37 1.644
124
GRS002 Gerstmann-Straussler-Scheinker Disease 36 1.644
125
DMN003 Dementia Familial British 30 1.644
126
c ALZ002 Alzheimer Disease Type 1 29 1.644
127
SHK001 Shaken Baby Syndrome 29 1.644
128
WSR001 Was-Related Disorders 22 1.644
129
GLC003 Glucose Intolerance 62 1.204
130
ACT019 Acute Myeloid Leukemia 87 1.162
131
P RHM011 Rheumatoid Arthritis 83 1.162
132
P ART022 Arthritis 75 1.162
133
SPS077 Sepsis 67 1.162
134
P NRM001 Neuromyelitis Optica 58 1.162
135
c HPT003 Hepatitis a 57 1.162
136
GLB015 Glioblastoma Multiforme 57 1.162
137
c ALZ003 Alzheimer Disease Type 2 57 1.162
138
P INF032 Infertility 55 1.162
139
RBS001 Rabies 51 1.162
140
P HYP027 Hypobetalipoproteinemia 51 1.162
141
HV1006 Hiv-1 42 1.162
142
INT063 Intellectual Disability 42 1.162
143
NSY001 N Syndrome 57 0.113
144
MNR012 M�ni�re Disease 28 0.087
145
LPD027 Lip Disease 23 0.087
146
P ATS008 Autosomal Dominant Disease 45 0.071
147
P HYP163 Hyperlipidemia Type 3 22 0.071
148
ALZ029 Alzheimer Disease Mitochondrial 15 0.071
149
P AST005 Asthma 86 0.050
150
P FML021 Familial Hypercholesterolemia 76 0.050
151
BRN106 Burns 61 0.050
152
MTR014 Motor Neuron Disease 56 0.050
153
HPT019 Hepatic Encephalopathy 51 0.050
154
c PRM010 Primary Open Angle Glaucoma 51 0.050
155
c LSS002 Lissencephaly 51 0.050
156
P OPN001 Open-Angle Glaucoma 51 0.050
157
P GLC007 Glaucoma 49 0.050
158
RHB003 Rhabdomyosarcoma 48 0.050
159
HMC014 Homocysteinemia 46 0.050
160
CRB004 Cerebral Artery Occlusion 45 0.050
161
HRD039 Hereditary Amyloidosis 42 0.050
162
LYM067 Lymphoid Leukemia 42 0.050
163
CRB008 Cerebral Atherosclerosis 39 0.050
164
NMN003 Niemann–pick Disease 29 0.050
165
APD001 Apo a-I Deficiency 26 0.050
166
c NMN006 Niemann-Pick Disease Type D 22 0.050