Search results for PVALB

75 hits were found for PVALB

# Family MCID Name MIFTS Score
1
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.538
2
P ALZ034 Alzheimer Disease 88 2.538
3
P SCH015 Schizophrenia 74 2.538
4
P EPL164 Epilepsy 71 2.538
5
CRT072 Creutzfeldt-Jakob Disease 70 2.538
6
P MTR014 Motor Neuron Disease 65 2.538
7
P FTL001 Fetal Alcohol Syndrome 57 2.538
8
P BPL003 Bipolar Disorder 56 2.538
9
GNG004 Ganglioglioma 54 2.538
10
FDL002 Food Allergy 51 2.538
11
P TMP001 Temporal Lobe Epilepsy 50 2.538
12
ONC007 Oncocytoma 49 2.538
13
SCR011 Scrapie 39 2.538
14
GTL001 Gitelman Syndrome 65 2.114
15
CHR177 Chromophobe Renal Cell Carcinoma 57 2.114
16
RNL114 Renal Cell Carcinoma, Nonpapillary 78 2.072
17
P PRK057 Parkinson Disease, Late-Onset 78 2.072
18
P TBR001 Tuberous Sclerosis 70 2.072
19
P SPR120 Supranuclear Palsy, Progressive, 1 68 2.072
20
P MJR001 Major Depressive Disorder 68 2.072
21
P MSC005 Muscular Dystrophy 66 2.072
22
P DYS154 Dystonia 65 2.072
23
WST001 West Syndrome 61 2.072
24
STT001 Status Epilepticus 60 2.072
25
P NMN002 Niemann-Pick Disease 59 2.072
26
GNG005 Gangliocytoma 55 2.072
27
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 2.072
28
c SPN294 Spinocerebellar Ataxia 1 53 2.072
29
CLL002 Collecting Duct Carcinoma 53 2.072
30
P RNL017 Renal Oncocytoma 53 2.072
31
P PRV002 Periventricular Nodular Heterotopia 52 2.072
32
c AML057 Amelogenesis Imperfecta, Type Iiia 40 2.072
33
NRX001 Neuroaxonal Dystrophy 35 2.072
34
FSH003 Fish Allergy 28 2.072
35
P RTN008 Retinitis Pigmentosa 79 1.465
36
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 1.465
37
P FRG001 Fragile X Syndrome 70 1.465
38
PSY004 Psychotic Disorder 67 1.465
39
GLL008 Gilles De La Tourette Syndrome 66 1.465
40
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 1.465
41
P ERL057 Early Infantile Epileptic Encephalopathy 63 1.465
42
P EPL140 Epilepsy, Idiopathic Generalized 62 1.465
43
P EPL198 Epilepsy, Myoclonic Juvenile 62 1.465
44
P CHL002 Childhood Absence Epilepsy 61 1.465
45
DSS008 Disease of Mental Health 58 1.465
46
P PRV006 Pervasive Developmental Disorder 57 1.465
47
KFM001 Kaufman Oculocerebrofacial Syndrome 56 1.465
48
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 1.465
49
FCL014 Focal Epilepsy 54 1.465
50
P TCD001 Tic Disorder 53 1.465
51
STT041 Stuttering 52 1.465
52
KGM001 Kagami-Ogata Syndrome 51 1.465
53
WRN002 Wernicke-Korsakoff Syndrome 50 1.465
54
AMB002 Amblyopia 49 1.465
55
SPC005 Speech Disorder 43 1.465
56
c FTL006 Fetal Alcohol Spectrum Disorder 43 1.465
57
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 1.465
58
ART014 Articulation Disorder 35 1.465
59
PRX097 Paroxysmal Dystonia 32 1.465
60
SPC003 Specific Developmental Disorder 31 1.465
61
P LTT001 Lattice Corneal Dystrophy 31 1.465
62
P ELC007 Electroclinical Syndrome 30 1.465
63
MLN063 Melon Allergy 25 1.465
64
CHL058 Childhood Electroclinical Syndrome 24 1.465
65
RNL009 Renal Pelvis Squamous Cell Carcinoma 24 1.465
66
NNT041 Neonatal Period Electroclinical Syndrome 23 1.465
67
BRS011 Breast Fibrosarcoma 20 1.465
68
ORN009 Orange Allergy 17 1.465
69
EPT024 Epithelial-Stromal Tgfbi Dystrophy 15 1.465
70
c ATS007 Autism Spectrum Disorder 67 0.113
71
P ATS364 Autism 70 0.092
72
THY029 Thyroid Carcinoma 59 0.092
73
P MDL005 Medulloblastoma 77 0.065
74
ADN018 Adenoma 59 0.065
75
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.065
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