Search results for "startle disease"

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

131 hits were found for 'startle disease'

# Family MCID Name MIFTS Score
1
P HYP097 Hyperekplexia 51 6.266
2
c HYP539 Hyperekplexia, Hereditary 1, Autosomal Dominant or Recessive 25 2.971
3
JMP002 Jumping Frenchmen of Maine 13 2.851
4
c EPL038 Epileptic Encephalopathy, Early Infantile, 8 24 2.838
5
P EPL164 Epilepsy 60 0.243
6
STR070 Startle Epilepsy 12 0.221
7
MYC033 Myoclonus 41 0.123
8
P SCH015 Schizophrenia 78 0.116
9
DSS008 Disease of Mental Health 48 0.109
10
P PRS038 Personality Disorder 60 0.106
11
ANX002 Anxiety Disorder 67 0.099
12
HMP005 Hemiplegia 52 0.097
13
P ENC018 Encephalopathy 59 0.094
14
CND002 Conduct Disorder 54 0.091
15
P DYS154 Dystonia 62 0.091
16
DMN002 Dementia 62 0.090
17
P CRV039 Cervicitis 45 0.088
18
NRN002 Neuronitis 40 0.088
19
ALC007 Alcohol Dependence 66 0.084
20
P TYS001 Tay-Sachs Disease 72 0.082
21
P ART022 Arthritis 73 0.080
22
DWN001 Down Syndrome 65 0.079
23
SCH011 Schizotypal Personality Disorder 32 0.076
24
PSY004 Psychotic Disorder 62 0.076
25
GLB003 Globe Disease 34 0.075
26
P RHM011 Rheumatoid Arthritis 87 0.074
27
SBS003 Substance Abuse 54 0.074
28
CRB009 Cerebritis 36 0.073
29
ASP002 Aspartylglucosaminuria 55 0.073
30
P OBS005 Obesity 91 0.073
31
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.072
32
P PNC025 Panic Disorder 60 0.072
33
PST028 Post-Traumatic Stress Disorder 55 0.071
34
ACT084 Acute Stress Disorder 38 0.071
35
DRG001 Drug Psychosis 39 0.071
36
MDD011 Mood Disorder 60 0.070
37
ALR002 Al-Raqad Syndrome 36 0.070
38
NTR005 Nutritional Deficiency Disease 51 0.070
39
RTR001 Retrograde Amnesia 40 0.070
40
P MYP004 Myopathy 67 0.069
41
CCN001 Cocaine Dependence 47 0.069
42
HYP144 Hyperacusis 22 0.069
43
SPS057 Spasticity 41 0.068
44
P MYM002 Moyamoya Disease 60 0.068
45
ATN002 Autonomic Nervous System Disease 46 0.067
46
ALN001 Aland Island Eye Disease 45 0.066
47
P MSC033 Muscle Disorders 52 0.064
48
MSC004 Muscle Tissue Disease 35 0.064
49
P HYP192 Hypocalcemia, Autosomal Dominant 50 0.064
50
GNR004 Generalized Anxiety Disorder 49 0.063
51
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.061
52
P FRG001 Fragile X Syndrome 68 0.061
53
P ANR007 Anorexia Nervosa 63 0.061
54
P CRN178 Coronary Heart Disease 6 22 0.061
55
DRG003 Drug Dependence 53 0.060
56
BLM002 Bulimia Nervosa 54 0.060
57
CRV043 Cervical Dystonia 43 0.059
58
P ATX004 Ataxia 53 0.059
59
P LNG032 Lung Cancer 92 0.059
60
SBS004 Substance Dependence 48 0.059
61
P GNR032 Generalized Dystonia 45 0.059
62
P TRM003 Tremor 54 0.059
63
CFF002 Coffin-Lowry Syndrome 56 0.059
64
CCN002 Cocaine Abuse 47 0.059
65
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.058
66
c HYP519 Hyperekplexia 3 22 0.058
67
c HYP536 Hyperekplexia 2, Autosomal Recessive 19 0.058
68
ANT011 Antisocial Personality Disorder 46 0.057
69
WHP002 Whiplash 35 0.056
70
c CLD016 Cold-Induced Sweating Syndrome 2 18 0.056
71
ATR060 Atrial Standstill, Digenic 51 0.054
72
WLL006 Wells Syndrome 57 0.054
73
WTH001 Withdrawal Disorder 36 0.053
74
GDS001 Good Syndrome 46 0.053
75
c CRN173 Coronary Heart Disease 8 19 0.053
76
PRD011 Proud Syndrome 42 0.053
77
NSD001 Nose Disease 51 0.052
78
ADL002 Adult Syndrome 53 0.052
79
AYM001 Ayme-Gripp Syndrome 40 0.051
80
PRC013 Pericarditis 52 0.051
81
ADT003 Auditory System Disease 49 0.050
82
BRN071 Brain Injury 51 0.050
83
RMS001 Rem Sleep Behavior Disorder 40 0.049
84
EXF001 Exfoliation Syndrome 56 0.049
85
CRB004 Cerebral Artery Occlusion 39 0.049
86
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 58 0.049
87
P PLN008 Peeling Skin Syndrome 45 0.049
88
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.049
89
MLR007 Male Reproductive System Disease 36 0.049
90
c CRN176 Coronary Heart Disease 9 19 0.049
91
RDN001 Reading Disorder 39 0.049
92
P INT063 Intellectual Disability 46 0.048
93
P TRN020 Turner Syndrome 64 0.048
94
MSC077 Muscle Eye Brain Disease 54 0.047
95
P CYS018 Cystitis 54 0.047
96
OVR063 Overnutrition 49 0.047
97
P PNT019 Pontocerebellar Hypoplasia 39 0.047
98
P PLL002 Pellagra 43 0.046
99
CNS002 Constrictive Pericarditis 31 0.046
100
c CNG031 Congenital Nervous System Abnormality 39 0.046
101
TRM010 Traumatic Brain Injury 52 0.046
102
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.045
103
P CHR084 Chromosomal Disease 37 0.045
104
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.045
105
P INT143 Interstitial Cystitis 57 0.045
106
DRG016 Drug Induced Dyskinesia 19 0.045
107
P PRD006 Prader-Willi Syndrome 64 0.044
108
STF001 Stiff-Person Syndrome 54 0.044
109
c GM2005 Gm2-Gangliosidosis, Ab Variant 32 0.044
110
OBS002 Obsessive-Compulsive Disorder 66 0.044
111
P EPS003 Episodic Ataxia 58 0.044
112
WSC001 Wisconsin Syndrome 16 0.044
113
HRT008 Heart Conduction Disease 43 0.044
114
P GNR027 Generalized Peeling Skin Syndrome 21 0.043
115
GLL008 Gilles De La Tourette Syndrome 63 0.043
116
c SCH051 Schizophrenia 4 36 0.043
117
P ATS007 Autism Spectrum Disorder 64 0.043
118
INT042 Internuclear Ophthalmoplegia 36 0.043
119
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 45 0.042
120
P BLP003 Blepharospasm 43 0.042
121
HYP264 Hypertonia 39 0.042
122
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 21 0.041
123
BRD004 Borderline Personality Disorder 46 0.041
124
c SCH056 Schizophrenia 15 25 0.041
125
ASP024 Asparagine Synthetase Deficiency 28 0.041
126
MLY001 Molybdenum Cofactor Deficiency 40 0.041
127
SPS061 Spastic Paraplegia, Optic Atrophy, and Neuropathy 22 0.041
128
OPT003 Opiate Dependence 49 0.040
129
ADG002 Audiogenic Seizures 21 0.040
130
SPN337 Spoan Syndrome 19 0.040
131
FRN002 Frontal Lobe Epilepsy 38 0.039