Search results for "startle disease"

The MalaCard for "startle disease" has been retired.
Searching MalaCards for entries containing "startle disease"

134 hits were found for 'startle disease'

# Family MCID Name MIFTS Score
1
c HYP539 Hyperekplexia, Hereditary 1, Autosomal Dominant or Recessive 47 7.613
2
c EPL038 Epileptic Encephalopathy, Early Infantile, 8 25 2.930
3
JMP002 Jumping Frenchmen of Maine 10 2.903
4
P EPL164 Epilepsy 66 0.242
5
STR070 Startle Epilepsy 12 0.219
6
MYC033 Myoclonus 41 0.115
7
P SCH015 Schizophrenia 76 0.114
8
P PRS038 Personality Disorder 61 0.105
9
ANX002 Anxiety Disorder 69 0.104
10
CND002 Conduct Disorder 56 0.102
11
NRN002 Neuronitis 42 0.102
12
DSS008 Disease of Mental Health 55 0.094
13
P DYS154 Dystonia 64 0.089
14
DMN002 Dementia 64 0.089
15
HMP005 Hemiplegia 54 0.088
16
P CRV039 Cervicitis 44 0.086
17
DRG001 Drug Psychosis 40 0.085
18
P TYS001 Tay-Sachs Disease 71 0.083
19
ALC007 Alcohol Dependence 65 0.083
20
PSY004 Psychotic Disorder 67 0.079
21
P ART022 Arthritis 75 0.079
22
P ENC018 Encephalopathy 59 0.077
23
P OBS005 Obesity 93 0.076
24
SCH011 Schizotypal Personality Disorder 33 0.075
25
GLB003 Globe Disease 35 0.074
26
P RHM011 Rheumatoid Arthritis 88 0.073
27
P TRM003 Tremor 54 0.073
28
SBS003 Substance Abuse 56 0.072
29
CRB009 Cerebritis 38 0.071
30
P PRP019 Peripheral Nervous System Disease 54 0.071
31
ACT084 Acute Stress Disorder 40 0.071
32
P PNC025 Panic Disorder 60 0.070
33
PST028 Post-Traumatic Stress Disorder 57 0.070
34
MDD011 Mood Disorder 61 0.069
35
NTR005 Nutritional Deficiency Disease 39 0.069
36
RTR001 Retrograde Amnesia 40 0.069
37
P MYP004 Myopathy 67 0.068
38
CCN001 Cocaine Dependence 48 0.068
39
P MYM002 Moyamoya Disease 60 0.067
40
HYP144 Hyperacusis 23 0.067
41
SPS057 Spasticity 42 0.067
42
DWN001 Down Syndrome 65 0.067
43
ATN002 Autonomic Nervous System Disease 47 0.066
44
ALN001 Aland Island Eye Disease 45 0.065
45
P MSC033 Muscle Disorders 52 0.064
46
BRN071 Brain Injury 52 0.064
47
MSC004 Muscle Tissue Disease 36 0.064
48
GNR004 Generalized Anxiety Disorder 51 0.062
49
ALR002 Al-Raqad Syndrome 36 0.062
50
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.061
51
ASP002 Aspartylglucosaminuria 59 0.061
52
P CRN178 Coronary Heart Disease 6 24 0.061
53
P FRG001 Fragile X Syndrome 68 0.060
54
TRM010 Traumatic Brain Injury 52 0.060
55
P LNG032 Lung Cancer 94 0.059
56
STF001 Stiff-Person Syndrome 56 0.059
57
P CLD010 Cold-Induced Sweating Syndrome 1 46 0.059
58
P ANR007 Anorexia Nervosa 63 0.059
59
CFF002 Coffin-Lowry Syndrome 55 0.059
60
DRG003 Drug Dependence 53 0.059
61
CRV043 Cervical Dystonia 44 0.058
62
c HYP519 Hyperekplexia 3 23 0.058
63
BLM002 Bulimia Nervosa 54 0.058
64
SBS004 Substance Dependence 50 0.058
65
c HYP536 Hyperekplexia 2, Autosomal Recessive 20 0.058
66
P ATX004 Ataxia 53 0.058
67
CCN002 Cocaine Abuse 47 0.057
68
OPS006 Opsoclonus-Myoclonus Syndrome 46 0.057
69
ANT011 Antisocial Personality Disorder 47 0.056
70
c CLD016 Cold-Induced Sweating Syndrome 2 20 0.056
71
WHP002 Whiplash 36 0.055
72
ATR060 Atrial Standstill, Digenic 53 0.054
73
WLL006 Wells Syndrome 56 0.054
74
GDS001 Good Syndrome 45 0.053
75
WTH001 Withdrawal Disorder 41 0.053
76
c CRN173 Coronary Heart Disease 8 20 0.053
77
PRD011 Proud Syndrome 42 0.052
78
NSD001 Nose Disease 52 0.052
79
c ESS001 Essential Tremor 61 0.051
80
P HYP192 Hypocalcemia, Autosomal Dominant 55 0.050
81
ADT003 Auditory System Disease 51 0.050
82
AYM001 Ayme-Gripp Syndrome 45 0.049
83
ADL002 Adult Syndrome 53 0.049
84
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 58 0.049
85
EXF001 Exfoliation Syndrome 57 0.049
86
P PLN008 Peeling Skin Syndrome 47 0.049
87
RMS001 Rem Sleep Behavior Disorder 40 0.049
88
PRC013 Pericarditis 52 0.049
89
CRB004 Cerebral Artery Occlusion 46 0.048
90
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.048
91
c CRN176 Coronary Heart Disease 9 20 0.048
92
MLR007 Male Reproductive System Disease 37 0.048
93
RDN001 Reading Disorder 39 0.048
94
MSC077 Muscle Eye Brain Disease 56 0.047
95
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.047
96
P INT063 Intellectual Disability 53 0.046
97
P PNT019 Pontocerebellar Hypoplasia 37 0.046
98
OVR063 Overnutrition 49 0.046
99
c CNG031 Congenital Nervous System Abnormality 39 0.046
100
P TRN020 Turner Syndrome 64 0.046
101
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.046
102
P CYS018 Cystitis 53 0.045
103
P PLL002 Pellagra 45 0.045
104
P CHR084 Chromosomal Disease 37 0.045
105
CNS002 Constrictive Pericarditis 34 0.045
106
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.045
107
c GM2005 Gm2-Gangliosidosis, Ab Variant 34 0.044
108
DRG016 Drug Induced Dyskinesia 21 0.044
109
P INT143 Interstitial Cystitis 57 0.044
110
WSC001 Wisconsin Syndrome 17 0.043
111
c SCH051 Schizophrenia 4 31 0.043
112
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 44 0.043
113
P PRD006 Prader-Willi Syndrome 63 0.043
114
c STR089 Striatal Degeneration, Autosomal Dominant 2 30 0.043
115
P GNR027 Generalized Peeling Skin Syndrome 22 0.043
116
OBS002 Obsessive-Compulsive Disorder 66 0.043
117
P EPS003 Episodic Ataxia 56 0.043
118
P ATS007 Autism Spectrum Disorder 64 0.042
119
HRT008 Heart Conduction Disease 43 0.042
120
GLL008 Gilles De La Tourette Syndrome 62 0.042
121
P EPS030 Episodic Kinesigenic Dyskinesia 1 27 0.042
122
P BLP003 Blepharospasm 44 0.042
123
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 0.042
124
HYP264 Hypertonia 40 0.041
125
INT042 Internuclear Ophthalmoplegia 36 0.041
126
c CLD017 Cold-Induced Sweating Syndrome 3 11 0.041
127
ASP024 Asparagine Synthetase Deficiency 27 0.041
128
c SCH056 Schizophrenia 15 26 0.041
129
MLY001 Molybdenum Cofactor Deficiency 40 0.040
130
SPS061 Spastic Paraplegia, Optic Atrophy, and Neuropathy 23 0.040
131
BRD004 Borderline Personality Disorder 46 0.040
132
ADG002 Audiogenic Seizures 25 0.040
133
SPN337 Spoan Syndrome 19 0.040
134
OPT003 Opiate Dependence 50 0.039