Search results for "[genes] PSEN1"

62 hits were found for '[genes] PSEN1'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 92 21.264
2
c ALZ036 Alzheimer Disease, Type 3 49 17.790
3
P DMN033 Dementia, Frontotemporal 63 16.471
4
c CRD112 Cardiomyopathy, Dilated, 1u 22 16.471
5
PCK002 Pick Disease 66 15.036
6
DMN002 Dementia 62 15.036
7
ACN011 Acne 63 13.448
8
P CRB019 Cerebral Amyloid Angiopathy 56 13.448
9
ACN016 Acne Inversa, Familial, 3 19 13.448
10
SPC010 Speech and Communication Disorders 42 11.647
11
P CRD011 Cardiomyopathy 66 11.647
12
APH002 Aphasia 52 11.647
13
HDR002 Hidradenitis Suppurativa 53 11.647
14
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 11.647
15
VSC002 Vascular Dementia 41 11.647
16
NRM002 Normal Pressure Hydrocephalus 47 11.647
17
HDR003 Hidradenitis 46 11.647
18
TPT001 Tauopathy 51 11.647
19
c AMY091 Amyotrophic Lateral Sclerosis 1 78 9.509
20
DMN031 Dementia, Lewy Body 58 9.509
21
P NRV007 Nervous System Disease 71 9.509
22
P AMY082 Amyloidosis, Familial Visceral 45 9.509
23
c ALZ035 Alzheimer Disease-4 35 9.509
24
KLV001 Kluver-Bucy Syndrome 37 9.509
25
c CNT035 Central Nervous System Disease 60 9.509
26
ALX001 Alexia 42 9.509
27
TRN012 Transient Global Amnesia 38 9.509
28
FTD003 Ftdals1 28 9.509
29
DYS003 Dysgraphia 34 9.509
30
ECH002 Echolalia 33 9.509
31
GTP001 Gait Apraxia 35 9.509
32
AMN003 Amnestic Disorder 45 9.509
33
ANT019 Anterograde Amnesia 35 9.509
34
P PRS013 Prosopagnosia 40 9.509
35
EXP001 Expressive Language Disorder 28 9.509
36
NMN001 Nominal Aphasia 28 9.509
37
IDM001 Ideomotor Apraxia 34 9.509
38
AGR018 Agraphia 38 9.509
39
BSL008 Basal Ganglia Disease 40 9.509
40
INT042 Internuclear Ophthalmoplegia 36 9.509
41
ANS006 Anosognosia 36 9.509
42
c ERL006 Early-Onset Familial Alzheimer Disease 36 9.509
43
SRC009 Sarcomatosis 36 9.509
44
VSL003 Visual Agnosia 27 9.509
45
c LTN003 Late-Onset Familial Alzheimer Disease 34 9.509
46
SPS019 Spastic Paraparesis 34 9.509
47
TPG001 Topographical Agnosia 8 9.509
48
APP006 Apperceptive Agnosia 15 9.509
49
PHN002 Phonagnosia 18 9.509
50
ASS001 Associative Agnosia 18 9.509
51
MPT001 Mapt-Related Disorders 17 9.509
52
WRT002 Writing Disorder 26 9.509
53
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 6.724
54
DSS008 Disease of Mental Health 48 6.724
55
SMN008 Semantic Dementia 43 6.724
56
c GRN014 Grn-Related Frontotemporal Dementia 36 6.724
57
FRN030 Frontotemporal Dementia with Parkinsonism-17 30 6.724
58
SPC003 Specific Developmental Disorder 39 6.724
59
BHV002 Behavioral Variant of Frontotemporal Dementia 37 6.724
60
FML304 Familial Isolated Dilated Cardiomyopathy 30 6.724
61
DSS024 Disease of Anatomical Entity 40 6.724
62
c PSN002 Psen1-Related Dilated Cardiomyopathy 9 6.724