Search results for htt

62 hits were found for htt

# Family MCID Name MIFTS Score
1
P HNT016 Huntington Disease 71 6.885
2
LPS021 Lopes-Maciel-Rodan Syndrome 21 4.332
3
P DYS154 Dystonia 65 2.936
4
P DMN002 Dementia 67 2.904
5
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.867
6
P PRK057 Parkinson Disease, Late-Onset 76 2.867
7
P PHC003 Pheochromocytoma 71 2.867
8
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 2.867
9
c SPN294 Spinocerebellar Ataxia 1 52 2.867
10
P MVM001 Movement Disease 61 2.384
11
P RTT002 Rett Syndrome 80 2.341
12
ACR006 Aceruloplasminemia 73 2.341
13
MLT157 Multiple System Atrophy 1 70 2.341
14
P FRG001 Fragile X Syndrome 68 2.341
15
PCK003 Pick Disease of Brain 68 2.341
16
P MCH002 Machado-Joseph Disease 63 2.341
17
ALX003 Alexander Disease 61 2.341
18
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 2.341
19
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 2.341
20
c SPN301 Spinocerebellar Ataxia 2 59 2.341
21
c HNT004 Huntington Disease-Like 2 49 2.341
22
CHR073 Choreatic Disease 52 1.712
23
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.655
24
P NRV007 Nervous System Disease 66 1.655
25
c MCP001 Mucopolysaccharidosis Iii 65 1.655
26
DMN031 Dementia, Lewy Body 65 1.655
27
P CHR071 Charcot-Marie-Tooth Disease 64 1.655
29
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 1.655
30
P PRN023 Prion Disease 57 1.655
31
GRS011 Gerstmann-Straussler Disease 55 1.655
32
MTC020 Mitochondrial Complex Ii Deficiency 54 1.655
33
c CNT035 Central Nervous System Disease 54 1.655
34
TXC002 Toxic Encephalopathy 52 1.655
35
MSC190 Muscular Disease 51 1.655
36
c EPL028 Epileptic Encephalopathy, Early Infantile, 5 45 1.655
37
KR002 Kuru 44 1.655
38
c SPN304 Spinocerebellar Ataxia 8 41 1.655
39
c SPS100 Spastic Paraplegia 38, Autosomal Dominant 40 1.655
40
c ALZ059 Alzheimer Disease 13 26 1.655
41
XLN228 X-Linked Recessive Disease 26 1.655
42
MDD001 Middle Cranial Fossa Meningioma 21 1.655
43
c XLN230 X-Linked Monogenic Disease 20 1.655
44
P ALZ034 Alzheimer Disease 88 0.097
45
HLX001 Helix Syndrome 47 0.097
46
P SCH015 Schizophrenia 75 0.069
47
SVR004 Severe Combined Immunodeficiency 73 0.069
48
P FRN006 Frontotemporal Dementia 70 0.069
49
ALC007 Alcohol Dependence 66 0.069
50
P MYP004 Myopathy 64 0.069
51
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.069
52
PRT013 Portal Hypertension 60 0.069
53
VRC005 Varicose Veins 60 0.069
54
STT001 Status Epilepticus 59 0.069
55
APH002 Aphasia 57 0.069
56
P TCD001 Tic Disorder 54 0.069
57
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.069
58
TLN003 Telangiectasis 51 0.069
59
c FNC029 Fanconi Anemia, Complementation Group I 50 0.069
60
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.069
61
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 39 0.069
62
c JVN015 Juvenile Huntington Disease 26 0.069
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