Search results for striatal degeneration

144 hits were found for striatal degeneration

# Family MCID Name MIFTS Score
1
c STR085 Striatonigral Degeneration, Infantile 27 7.071
2
P STR101 Striatal Degeneration, Autosomal Dominant 1 23 6.545
3
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 22 5.511
4
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 4.567
5
STR099 Striatonigral Degeneration, Infantile, Mitochondrial 15 4.060
6
c SPR070 Sporadic Infantile Bilateral Striatal Necrosis 9 3.030
7
c FML309 Familial Infantile Bilateral Striatal Necrosis 12 2.398
8
NRN002 Neuronitis 43 0.680
9
AGN016 Aging 65 0.573
10
P CRB059 Cerebellar Degeneration 40 0.314
11
WLL004 Wallerian Degeneration 40 0.304
12
CRT033 Corticobasal Degeneration 51 0.291
13
P DYS154 Dystonia 61 0.234
14
CRB009 Cerebritis 41 0.234
15
P ALZ034 Alzheimer Disease 95 0.233
16
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.214
17
MLT157 Multiple System Atrophy 1 65 0.214
18
P STR001 Striatonigral Degeneration 34 0.211
19
DMN002 Dementia 68 0.208
20
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 0.207
21
P SCH015 Schizophrenia 71 0.194
22
CHR073 Choreatic Disease 40 0.172
23
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.172
24
ISC004 Ischemia 66 0.167
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.161
26
P LTR001 Lateral Sclerosis 58 0.153
27
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.152
28
P PRK057 Parkinson Disease, Late-Onset 78 0.147
29
c BLD140 Blood Group, I System 37 0.145
30
P HNT016 Huntington Disease 78 0.135
31
FRN006 Frontotemporal Dementia 70 0.134
32
P OLV001 Olivopontocerebellar Atrophy 51 0.132
33
MYC033 Myoclonus 40 0.128
34
P TRM003 Tremor 54 0.123
35
P NRP001 Neuropathy 63 0.123
36
P CRV039 Cervicitis 49 0.122
37
P EPL164 Epilepsy 70 0.122
38
PCK003 Pick Disease of Brain 66 0.118
39
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.113
40
P ENC004 Encephalitis 66 0.107
41
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.106
42
P NRN021 Neuronal Ceroid Lipofuscinosis 62 0.106
43
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.106
44
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.106
45
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.106
46
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.106
47
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.106
48
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.106
49
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.106
50
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.106
51
P ANR048 Aniridia 1 68 0.104
52
ANR038 Anorexia Nervosa 1 21 0.102
53
BLD137 Blood Group--Ahonen 17 0.102
54
P ENC018 Encephalopathy 58 0.101
55
BSL008 Basal Ganglia Disease 44 0.100
56
MVM001 Movement Disease 40 0.100
57
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.100
58
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.100
59
BLD149 Blood Group--Rhesus System E Polypeptide 16 0.098
60
APR001 Apraxia 52 0.098
61
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.097
62
P MCH002 Machado-Joseph Disease 63 0.096
63
HYP266 Hypoxia 61 0.095
64
RMS001 Rem Sleep Behavior Disorder 42 0.095
65
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 42 0.094
66
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.093
67
APH002 Aphasia 58 0.092
68
PTH002 Pathological Gambling 53 0.087
69
P MLT020 Multiple Sclerosis 85 0.087
70
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.087
71
ANX010 Anxiety 72 0.082
72
P HPT021 Hepatitis 75 0.081
73
P PRS038 Personality Disorder 65 0.081
74
P BPL003 Bipolar Disorder 61 0.079
75
c CNT035 Central Nervous System Disease 65 0.078
76
CRB004 Cerebral Artery Occlusion 46 0.077
77
P NRV007 Nervous System Disease 75 0.076
78
WLS001 Wilson Disease 72 0.075
79
CRT072 Creutzfeldt-Jakob Disease 65 0.075
80
LMB024 Limbic Encephalitis 42 0.074
81
TRN015 Transient Cerebral Ischemia 58 0.074
82
P GLT035 Glutaric Acidemia I 40 0.074
83
c ESS001 Essential Tremor 58 0.072
84
P HYD006 Hydrocephalus 68 0.070
85
STF001 Stiff-Person Syndrome 61 0.070
86
c SPN294 Spinocerebellar Ataxia 1 58 0.067
87
BRN071 Brain Injury 54 0.067
88
HPT082 Hepatic Adenomas, Familial 52 0.067
89
SYN058 Synucleinopathy 42 0.067
90
P PNM007 Pneumonia 70 0.065
91
GLL008 Gilles De La Tourette Syndrome 64 0.065
92
TMP001 Temporal Lobe Epilepsy 54 0.065
93
CCN001 Cocaine Dependence 52 0.065
94
CCN002 Cocaine Abuse 50 0.065
95
LGH007 Leigh Syndrome 68 0.064
96
P AST007 Astrocytoma 66 0.064
97
DMN031 Dementia, Lewy Body 66 0.064
98
c HYP699 Hyperekplexia 1 25 0.064
99
STT001 Status Epilepticus 60 0.063
100
P THY032 Thyroiditis 56 0.063
101
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.063
102
TRM010 Traumatic Brain Injury 54 0.061
103
STR093 Striatonigral Degeneration, Childhood-Onset 19 0.061
104
RST001 Restless Legs Syndrome 54 0.060
105
P BLP003 Blepharospasm 46 0.060
106
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.059
107
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 0.059
108
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.057
109
ATN005 Autonomic Dysfunction 51 0.057
110
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.057
111
P FRG001 Fragile X Syndrome 69 0.055
112
LSC001 Lesch-Nyhan Syndrome 62 0.055
113
P GLM045 Glioma 61 0.055
114
HYD061 Hydrocephalus, Normal-Pressure 47 0.055
115
MCL009 Mcleod Syndrome 45 0.055
116
EXT039 Extrapontine Myelinolysis 18 0.055
117
MDD011 Mood Disorder 64 0.054
118
P HMP006 Hemiplegic Migraine 49 0.051
119
DNC004 Diencephalic Syndrome 37 0.051
120
MNG003 Mungan Syndrome 34 0.051
121
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 32 0.051
122
HMN044 Human Immunodeficiency Virus Type 1 71 0.047
123
HYP056 Hypoglycemia 62 0.047
124
MGR028 Migraine with or Without Aura 1 55 0.047
125
CRB090 Cerebral Hypoxia 47 0.047
126
BRN018 Borna Disease 38 0.047
127
ALL014 Allergic Encephalomyelitis 37 0.047
128
MRC001 Marchiafava Bignami Disease 23 0.047
129
SHW002 Shwachman-Diamond Syndrome 63 0.042
130
P ALC004 Alcohol Abuse 63 0.042
131
P HYP086 Hypothyroidism 62 0.042
132
PRT058 Pure Autonomic Failure 60 0.042
133
HPT019 Hepatic Encephalopathy 59 0.042
134
BRN106 Burns 57 0.042
135
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 54 0.042
136
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.042
137
P LCT001 Lactic Acidosis 51 0.042
138
CHR105 Choreoacanthocytosis 46 0.042
139
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 41 0.042
140
RDN001 Reading Disorder 36 0.042
141
PND004 Pandas 34 0.042
142
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.042
143
CLF028 Cleft Soft Palate 30 0.042
144
PRM157 Primary Progressive Freezing Gait 9 0.042
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