Search results for striatal degeneration

139 hits were found for striatal degeneration

# Family MCID Name MIFTS Score
1
P STR045 Striatal Degeneration, Autosomal Dominant 25 6.082
2
c STR085 Striatonigral Degeneration, Infantile 22 5.867
3
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 26 5.212
4
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 3.375
5
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 10 3.354
6
c FML309 Familial Infantile Bilateral Striatal Necrosis 13 2.403
7
c SPR070 Sporadic Infantile Bilateral Striatal Necrosis 7 2.380
8
NRN002 Neuronitis 41 0.641
9
P CRB059 Cerebellar Degeneration 34 0.273
10
WLL004 Wallerian Degeneration 36 0.265
11
P CRT033 Corticobasal Degeneration 47 0.256
12
P DYS154 Dystonia 65 0.221
13
CRB009 Cerebritis 39 0.212
14
MLT021 Multiple System Atrophy 70 0.201
15
P STR001 Striatonigral Degeneration 28 0.200
16
P SCH015 Schizophrenia 77 0.194
17
GLB003 Globe Disease 32 0.192
18
DMN002 Dementia 65 0.189
19
ISC004 Ischemia 61 0.158
20
P ATX004 Ataxia 53 0.149
21
P LTR001 Lateral Sclerosis 53 0.135
22
P HNT016 Huntington Disease 80 0.132
23
OLV001 Olivopontocerebellar Atrophy 53 0.125
24
P CRV039 Cervicitis 45 0.115
25
P TRM003 Tremor 54 0.111
26
MYC033 Myoclonus 42 0.111
27
P NRP001 Neuropathy 59 0.108
28
MVM001 Movement Disease 49 0.108
29
P EPL164 Epilepsy 66 0.106
30
P NRN021 Neuronal Ceroid Lipofuscinosis 59 0.100
31
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.100
32
P ALZ034 Alzheimer Disease 92 0.098
33
P ENC018 Encephalopathy 59 0.098
34
BSL008 Basal Ganglia Disease 40 0.095
35
P ENC004 Encephalitis 63 0.095
36
P MCH002 Machado-Joseph Disease 63 0.092
37
P OBS005 Obesity 92 0.091
38
OCL011 Ocular Motility Disease 37 0.091
39
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.089
40
HYP266 Hypoxia 56 0.088
41
APR001 Apraxia 51 0.086
42
HV1006 Hiv-1 80 0.086
43
RDN001 Reading Disorder 34 0.086
44
OPT006 Optic Nerve Disease 52 0.085
45
FST001 Foster-Kennedy Syndrome 31 0.085
46
APH002 Aphasia 54 0.083
47
RMS001 Rem Sleep Behavior Disorder 41 0.082
48
ALC007 Alcohol Dependence 63 0.079
49
P PRS038 Personality Disorder 62 0.079
50
DRG001 Drug Psychosis 38 0.079
51
P PRK057 Parkinson Disease, Late-Onset 70 0.078
52
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.073
53
CRB004 Cerebral Artery Occlusion 45 0.073
54
WLS001 Wilson Disease 72 0.072
55
P HPT021 Hepatitis 69 0.072
56
LPD004 Lipoid Nephrosis 48 0.072
57
P MYP004 Myopathy 67 0.071
58
TRN015 Transient Cerebral Ischemia 56 0.071
59
P BPL003 Bipolar Disorder 62 0.066
60
STF001 Stiff-Person Syndrome 56 0.066
61
DSS008 Disease of Mental Health 52 0.066
62
ATN002 Autonomic Nervous System Disease 48 0.066
63
P HYD006 Hydrocephalus 66 0.064
64
c ESS001 Essential Tremor 59 0.064
65
SYN058 Synucleinopathy 38 0.064
66
P CRT072 Creutzfeldt-Jakob Disease 61 0.062
67
P PNM007 Pneumonia 68 0.059
68
NRM002 Normal Pressure Hydrocephalus 50 0.058
69
P BLP003 Blepharospasm 43 0.058
70
STT001 Status Epilepticus 59 0.057
71
BRN071 Brain Injury 52 0.057
72
LMB024 Limbic Encephalitis 38 0.057
73
MSC004 Muscle Tissue Disease 34 0.057
74
P THY032 Thyroiditis 54 0.055
75
P MSC033 Muscle Disorders 52 0.055
76
PHY002 Physical Disorder 43 0.055
77
STR093 Striatonigral Degeneration, Childhood-Onset 9 0.055
78
P LGH007 Leigh Syndrome 70 0.054
79
P HLP001 Holoprosencephaly 63 0.054
80
LSC001 Lesch-Nyhan Syndrome 61 0.054
81
P GLM045 Glioma 60 0.054
82
P ALC004 Alcohol Abuse 59 0.054
83
RST001 Restless Legs Syndrome 54 0.054
84
EXT039 Extrapontine Myelinolysis 15 0.054
85
P MCL013 Mucolipidosis Iv 62 0.053
86
ATN005 Autonomic Dysfunction 49 0.053
87
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.053
88
P TYS001 Tay-Sachs Disease 71 0.051
89
TRM010 Traumatic Brain Injury 52 0.051
90
HYP056 Hypoglycemia 61 0.048
91
c CNT035 Central Nervous System Disease 60 0.048
92
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 57 0.048
93
EXF001 Exfoliation Syndrome 57 0.048
94
P HMP006 Hemiplegic Migraine 45 0.048
95
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.048
96
ANX002 Anxiety Disorder 67 0.045
97
P AST007 Astrocytoma 65 0.045
98
HYP037 Hyperhomocysteinemia 50 0.045
99
P PLN008 Peeling Skin Syndrome 45 0.045
100
CRB090 Cerebral Hypoxia 45 0.045
101
SPH010 Sphingolipidosis 45 0.045
102
BRN018 Borna Disease 42 0.045
103
MRC001 Marchiafava Bignami Disease 39 0.045
104
c CNG031 Congenital Nervous System Abnormality 37 0.045
105
c PLN017 Peeling Skin Syndrome 1 34 0.045
106
P GNG010 Gangliosidosis Gm2 32 0.045
107
MLR004 Malaria 83 0.041
108
P HYP086 Hypothyroidism 64 0.041
109
SHW002 Shwachman-Diamond Syndrome 61 0.041
110
HPT019 Hepatic Encephalopathy 56 0.041
111
PLL001 Pallister-Hall Syndrome 55 0.041
112
c VRL007 Viral Encephalitis 54 0.041
113
AGN012 Agnathia-Otocephaly Complex 53 0.041
114
SNG010 Single Median Maxillary Central Incisor 52 0.041
115
BRN106 Burns 52 0.041
116
PRT058 Pure Autonomic Failure 52 0.041
117
c PRK031 Parkinson Disease 1 51 0.041
118
P LCT001 Lactic Acidosis 51 0.041
119
OVR063 Overnutrition 50 0.041
120
P INT063 Intellectual Disability 49 0.041
121
MSS002 Mass Syndrome 48 0.041
122
CHR105 Choreoacanthocytosis 44 0.041
123
c BRD044 Bardet-Biedl Syndrome 17 44 0.041
124
INF039 Infratentorial Cancer 42 0.041
125
c PLN018 Peeling Skin Syndrome 2 40 0.041
126
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 39 0.041
127
CHR211 Chromosome 18p Deletion Syndrome 38 0.041
128
SML028 Semilobar Holoprosencephaly 37 0.041
129
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 36 0.041
130
NNL001 Non-Langerhans-Cell Histiocytosis 36 0.041
131
ALB014 Alobar Holoprosencephaly 35 0.041
132
LBR025 Lobar Holoprosencephaly 34 0.041
133
ALL014 Allergic Encephalomyelitis 32 0.041
134
c ALZ043 Alzheimer's Disease 15 32 0.041
135
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 29 0.041
136
c PRK026 Parkinson Disease 11 29 0.041
137
SPT016 Septopreoptic Holoprosencephaly 29 0.041
138
PND004 Pandas 29 0.041
139
18P001 18p Deletion Syndrome 22 0.041
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