Search results for "[genes] PSEN1"

60 hits were found for '[genes] PSEN1'

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 92 20.310
2
PCK002 Pick Disease 68 19.148
3
P DMN033 Dementia, Frontotemporal 62 19.148
4
c ALZ036 Alzheimer Disease, Type 3 53 19.148
5
DMN002 Dementia 65 17.911
6
P AMY004 Amyloidosis 65 15.138
7
P CRB019 Cerebral Amyloid Angiopathy 58 15.138
8
VSC002 Vascular Dementia 54 15.138
9
c CRD112 Cardiomyopathy, Dilated, 1u 23 15.138
10
ACN016 Acne Inversa, Familial, 3 19 15.138
11
APH002 Aphasia 54 13.540
12
NRM002 Normal Pressure Hydrocephalus 50 13.540
13
HDR003 Hidradenitis 45 13.540
14
SPC010 Speech and Communication Disorders 41 13.540
15
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 13.540
16
c ERL006 Early-Onset Familial Alzheimer Disease 37 13.540
17
c AMY091 Amyotrophic Lateral Sclerosis 1 78 11.726
18
P NRV007 Nervous System Disease 71 11.726
19
P CRD011 Cardiomyopathy 68 11.726
20
ACN011 Acne 62 11.726
21
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 11.726
22
c ALZ037 Alzheimer Disease-2 52 11.726
23
HDR002 Hidradenitis Suppurativa 51 11.726
24
P AMY082 Amyloidosis, Familial Visceral 45 11.726
25
c ALZ035 Alzheimer Disease-4 45 11.726
26
SMN008 Semantic Dementia 44 11.726
27
AMN003 Amnestic Disorder 43 11.726
28
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 11.726
29
SPS019 Spastic Paraparesis 41 11.726
30
ALX001 Alexia 40 11.726
31
BSL008 Basal Ganglia Disease 40 11.726
32
ANL004 Anal Canal Squamous Cell Carcinoma 39 11.726
33
TRN012 Transient Global Amnesia 39 11.726
34
BHV002 Behavioral Variant of Frontotemporal Dementia 39 11.726
35
KLV001 Kluver-Bucy Syndrome 38 11.726
36
INT042 Internuclear Ophthalmoplegia 37 11.726
37
IDM001 Ideomotor Apraxia 36 11.726
38
AGR018 Agraphia 36 11.726
39
DYS003 Dysgraphia 36 11.726
40
GTP001 Gait Apraxia 35 11.726
41
NMN001 Nominal Aphasia 33 11.726
42
PRS013 Prosopagnosia 31 11.726
43
ECH002 Echolalia 30 11.726
44
EXP001 Expressive Language Disorder 29 11.726
45
WRT002 Writing Disorder 27 11.726
46
VSL003 Visual Agnosia 26 11.726
47
ASS001 Associative Agnosia 17 11.726
48
PHN002 Phonagnosia 17 11.726
49
MPT001 Mapt-Related Disorders 16 11.726
50
APP006 Apperceptive Agnosia 14 11.726
51
c PSN002 Psen1-Related Dilated Cardiomyopathy 10 11.726
52
TPG001 Topographical Agnosia 6 11.726
53
c DLT002 Dilated Cardiomyopathy 76 9.574
54
c CNT035 Central Nervous System Disease 60 9.574
55
DMN031 Dementia, Lewy Body 58 9.574
56
DSS008 Disease of Mental Health 52 9.574
57
c GRN014 Grn-Related Frontotemporal Dementia 40 9.574
58
SPC003 Specific Developmental Disorder 38 9.574
59
FML304 Familial Isolated Dilated Cardiomyopathy 31 9.574
60
FRN030 Frontotemporal Dementia with Parkinsonism-17 29 9.574