Search results for "[genes] PSEN1"

63 hits were found for '[genes] PSEN1'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 91 19.076
2
PCK002 Pick Disease 58 16.521
3
P DMN033 Dementia, Frontotemporal 57 16.521
4
DMN002 Dementia 51 16.521
5
c ALZ036 Alzheimer Disease, Type 3 41 16.521
6
c CRD112 Cardiomyopathy, Dilated, 1u 22 16.521
7
P AMY004 Amyloidosis 59 13.489
8
VSC002 Vascular Dementia 48 13.489
9
ACN016 Acne Inversa, Familial, 3 19 13.489
10
P CRD011 Cardiomyopathy 59 11.682
11
P CRB019 Cerebral Amyloid Angiopathy 56 11.682
12
ACN011 Acne 55 11.682
13
HDR002 Hidradenitis Suppurativa 48 11.682
14
TPT001 Tauopathy 43 11.682
15
HDR003 Hidradenitis 39 11.682
16
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 29 11.682
17
SPC010 Speech and Communication Disorders 29 11.682
18
c AMY091 Amyotrophic Lateral Sclerosis 1 74 9.538
19
P NRV007 Nervous System Disease 51 9.538
20
c ALZ037 Alzheimer Disease-2 47 9.538
21
P AMY082 Amyloidosis, Familial Visceral 40 9.538
22
P PRS013 Prosopagnosia 39 9.538
23
TRN012 Transient Global Amnesia 38 9.538
24
ALX001 Alexia 37 9.538
25
AMN003 Amnestic Disorder 36 9.538
26
INT042 Internuclear Ophthalmoplegia 36 9.538
27
ANS006 Anosognosia 34 9.538
28
IDM001 Ideomotor Apraxia 34 9.538
29
KLV001 Kluver-Bucy Syndrome 33 9.538
30
KHL003 Kohlschutter-Tonz Syndrome 33 9.538
31
AGR018 Agraphia 32 9.538
32
SRC009 Sarcomatosis 32 9.538
33
ANT019 Anterograde Amnesia 32 9.538
34
DYS003 Dysgraphia 31 9.538
35
BSL008 Basal Ganglia Disease 29 9.538
36
c ALZ002 Alzheimer Disease Type 1 29 9.538
37
ECH002 Echolalia 28 9.538
38
VSL003 Visual Agnosia 28 9.538
39
SPS019 Spastic Paraparesis 26 9.538
40
NMN001 Nominal Aphasia 25 9.538
41
FTD003 Ftdals1 23 9.538
42
GTP001 Gait Apraxia 22 9.538
43
EXP001 Expressive Language Disorder 21 9.538
44
WRT002 Writing Disorder 19 9.538
45
APP006 Apperceptive Agnosia 19 9.538
46
ASS001 Associative Agnosia 19 9.538
47
PHN002 Phonagnosia 18 9.538
48
MPT001 Mapt-Related Disorders 15 9.538
49
TPG001 Topographical Agnosia 6 9.538
50
DMN031 Dementia, Lewy Body 54 6.745
51
c CNT035 Central Nervous System Disease 48 6.745
52
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 47 6.745
53
DSS008 Disease of Mental Health 39 6.745
54
SMN008 Semantic Dementia 37 6.745
55
c ALZ035 Alzheimer Disease-4 37 6.745
56
DSS024 Disease of Anatomical Entity 34 6.745
57
FML304 Familial Isolated Dilated Cardiomyopathy 30 6.745
58
SPC003 Specific Developmental Disorder 30 6.745
59
PRG033 Progressive Non-Fluent Aphasia 29 6.745
60
c GRN014 Grn-Related Frontotemporal Dementia 28 6.745
61
BHV002 Behavioral Variant of Frontotemporal Dementia 27 6.745
62
FRN030 Frontotemporal Dementia with Parkinsonism-17 22 6.745
63
c PSN002 Psen1-Related Dilated Cardiomyopathy 9 6.745