Search results for "[genes] PSEN1"

63 hits were found for '[genes] PSEN1'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 94 19.076
2
PCK002 Pick Disease 65 16.521
3
DMN002 Dementia 64 16.521
4
P DMN033 Dementia, Frontotemporal 62 16.521
5
c ALZ036 Alzheimer Disease, Type 3 47 16.521
6
c CRD112 Cardiomyopathy, Dilated, 1u 19 16.521
7
P AMY004 Amyloidosis 68 13.489
8
VSC002 Vascular Dementia 58 13.489
9
ACN016 Acne Inversa, Familial, 3 17 13.489
10
P CRD011 Cardiomyopathy 68 11.682
11
ACN011 Acne 65 11.682
12
P CRB019 Cerebral Amyloid Angiopathy 56 11.682
13
HDR002 Hidradenitis Suppurativa 55 11.682
14
TPT001 Tauopathy 54 11.682
15
HDR003 Hidradenitis 47 11.682
16
SPC010 Speech and Communication Disorders 45 11.682
17
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 33 11.682
18
c AMY091 Amyotrophic Lateral Sclerosis 1 79 9.538
19
P NRV007 Nervous System Disease 70 9.538
20
c ALZ037 Alzheimer Disease-2 57 9.538
21
AMN003 Amnestic Disorder 50 9.538
22
P AMY082 Amyloidosis, Familial Visceral 48 9.538
23
KHL003 Kohlschutter-Tonz Syndrome 48 9.538
24
ALX001 Alexia 48 9.538
25
TRN012 Transient Global Amnesia 44 9.538
26
P PRS013 Prosopagnosia 43 9.538
27
c ALZ002 Alzheimer Disease Type 1 43 9.538
28
INT042 Internuclear Ophthalmoplegia 41 9.538
29
BSL008 Basal Ganglia Disease 40 9.538
30
ANT019 Anterograde Amnesia 40 9.538
31
ANS006 Anosognosia 39 9.538
32
KLV001 Kluver-Bucy Syndrome 38 9.538
33
AGR018 Agraphia 38 9.538
34
SRC009 Sarcomatosis 37 9.538
35
IDM001 Ideomotor Apraxia 37 9.538
36
DYS003 Dysgraphia 36 9.538
37
ECH002 Echolalia 35 9.538
38
GTP001 Gait Apraxia 33 9.538
39
NMN001 Nominal Aphasia 33 9.538
40
SPS019 Spastic Paraparesis 32 9.538
41
EXP001 Expressive Language Disorder 32 9.538
42
FTD003 Ftdals1 30 9.538
43
VSL003 Visual Agnosia 29 9.538
44
WRT002 Writing Disorder 28 9.538
45
ASS001 Associative Agnosia 21 9.538
46
APP006 Apperceptive Agnosia 19 9.538
47
PHN002 Phonagnosia 19 9.538
48
MPT001 Mapt-Related Disorders 19 9.538
49
TPG001 Topographical Agnosia 10 9.538
50
c CNT035 Central Nervous System Disease 61 6.745
51
DMN031 Dementia, Lewy Body 60 6.745
52
DSS008 Disease of Mental Health 56 6.745
53
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 51 6.745
54
SMN008 Semantic Dementia 46 6.745
55
DSS024 Disease of Anatomical Entity 43 6.745
56
c GRN014 Grn-Related Frontotemporal Dementia 43 6.745
57
SPC003 Specific Developmental Disorder 41 6.745
58
FML304 Familial Isolated Dilated Cardiomyopathy 34 6.745
59
c ALZ035 Alzheimer Disease-4 33 6.745
60
PRG033 Progressive Non-Fluent Aphasia 33 6.745
61
FRN030 Frontotemporal Dementia with Parkinsonism-17 33 6.745
62
BHV002 Behavioral Variant of Frontotemporal Dementia 32 6.745
63
c PSN002 Psen1-Related Dilated Cardiomyopathy 10 6.745