Search results for "[genes] PSEN1"

66 hits were found for '[genes] PSEN1'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 98 21.170
2
DMN002 Dementia 53 17.712
3
PCK002 Pick Disease 61 16.398
4
P DMN033 Dementia, Frontotemporal 59 16.398
5
c ALZ036 Alzheimer Disease, Type 3 43 16.398
6
TPT001 Tauopathy 42 16.398
7
c CRD112 Cardiomyopathy, Dilated, 1u 22 16.398
8
P AMY004 Amyloidosis 60 14.969
9
P CRB019 Cerebral Amyloid Angiopathy 56 13.389
10
c CNT035 Central Nervous System Disease 52 13.389
11
PRN023 Prion Disease 50 13.389
12
HDR002 Hidradenitis Suppurativa 48 13.389
13
VSC002 Vascular Dementia 47 13.389
14
HDR003 Hidradenitis 38 13.389
15
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 27 13.389
16
ACN016 Acne Inversa, Familial, 3 19 13.389
17
c DLT002 Dilated Cardiomyopathy 73 11.595
18
P CNG401 Congenital Heart Disease 68 11.595
19
ACN011 Acne 55 11.595
20
P CRD011 Cardiomyopathy 53 11.595
21
P NRV007 Nervous System Disease 49 11.595
22
NRM002 Normal Pressure Hydrocephalus 49 11.595
23
SPC010 Speech and Communication Disorders 31 11.595
24
SWT003 Sweat Gland Disease 25 11.595
25
c AMY091 Amyotrophic Lateral Sclerosis 1 83 9.468
26
CNG034 Congestive Heart Failure 65 9.468
27
c ALZ037 Alzheimer Disease-2 52 9.468
28
P AMY082 Amyloidosis, Familial Visceral 43 9.468
29
TRN012 Transient Global Amnesia 39 9.468
30
P PRS013 Prosopagnosia 38 9.468
31
ALX001 Alexia 36 9.468
32
KLV001 Kluver-Bucy Syndrome 36 9.468
33
DYS003 Dysgraphia 36 9.468
34
ANS006 Anosognosia 36 9.468
35
IDM001 Ideomotor Apraxia 34 9.468
36
RTR001 Retrograde Amnesia 34 9.468
37
SRC009 Sarcomatosis 34 9.468
38
INT042 Internuclear Ophthalmoplegia 34 9.468
39
AGR018 Agraphia 33 9.468
40
FTD003 Ftdals1 33 9.468
41
AMN003 Amnestic Disorder 32 9.468
42
BSL008 Basal Ganglia Disease 32 9.468
43
ECH002 Echolalia 31 9.468
44
ANT019 Anterograde Amnesia 31 9.468
45
NMN001 Nominal Aphasia 29 9.468
46
VSL003 Visual Agnosia 28 9.468
47
SPS019 Spastic Paraparesis 27 9.468
48
EXP001 Expressive Language Disorder 22 9.468
49
GTP001 Gait Apraxia 21 9.468
50
ASS001 Associative Agnosia 19 9.468
51
WRT002 Writing Disorder 19 9.468
52
PHN002 Phonagnosia 18 9.468
53
MPT001 Mapt-Related Disorders 17 9.468
54
APP006 Apperceptive Agnosia 16 9.468
55
c PSN002 Psen1-Related Dilated Cardiomyopathy 10 9.468
56
TPG001 Topographical Agnosia 5 9.468
57
DMN031 Dementia, Lewy Body 53 6.695
58
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 48 6.695
59
c ALZ035 Alzheimer Disease-4 39 6.695
60
SMN008 Semantic Dementia 37 6.695
61
c GRN014 Grn-Related Frontotemporal Dementia 36 6.695
62
c FNC042 Fanconi Anemia, Complementation Group D2 35 6.695
63
FML304 Familial Isolated Dilated Cardiomyopathy 31 6.695
64
PRG033 Progressive Non-Fluent Aphasia 28 6.695
65
BHV002 Behavioral Variant of Frontotemporal Dementia 26 6.695
66
FRN030 Frontotemporal Dementia with Parkinsonism-17 22 6.695