Search results for tubg1

61 hits were found for tubg1

# Family MCID Name MIFTS Score
1
c CRT071 Cortical Dysplasia, Complex, with Other Brain Malformations 4 22 36.036
2
P LSS002 Lissencephaly 53 18.199
3
P MCR010 Microcephaly 59 15.072
4
P BND018 Band Heterotopia 53 11.027
5
P JBR020 Joubert Syndrome 1 74 10.724
6
P RTN008 Retinitis Pigmentosa 79 10.724
7
P TRC102 Trichothiodystrophy 1, Photosensitive 49 10.724
8
TKL001 Tukel Syndrome 52 7.975
9
P PRV002 Periventricular Nodular Heterotopia 52 7.758
10
c LSS006 Lissencephaly 2 54 7.583
11
c FNC027 Fanconi Anemia, Complementation Group a 81 7.583
12
MLL018 Miller-Dieker Lissencephaly Syndrome 53 7.583
13
P BRT040 Baraitser-Winter Syndrome 34 7.583
14
IMM172 Immunodeficiency 34 28 7.583
15
WLK001 Walker-Warburg Syndrome 62 7.583
16
c CNG031 Congenital Nervous System Abnormality 24 7.583
17
c PRM031 Primary Autosomal Recessive Microcephaly 55 7.583
18
P RDC010 Reducing Body Myopathy 33 7.583
19
TBL035 Tubulinopathy 34 2.106
20
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 2.062
21
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.062
22
P BRS047 Breast Cancer 97 1.793
23
PCH002 Pachygyria 32 1.380
24
c LSS005 Lissencephaly 1 57 1.262
26
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.149
27
HYP264 Hypertonia 36 1.149
28
c MNT143 Mental Retardation, Autosomal Dominant 13 34 1.047
29
c CRT068 Cortical Dysplasia, Complex, with Other Brain Malformations 3 24 1.047
30
c SPN385 Spinal Muscular Atrophy, Lower Extremity-Predominant, 1, Autosomal Dominant 31 1.047
31
c CRT067 Cortical Dysplasia, Complex, with Other Brain Malformations 2 32 1.047
32
ATS237 Autosomal Dominant Childhood-Onset Proximal Spinal Muscular Atrophy 24 1.047
33
P PNC035 Pancreatic Cancer 86 0.602
34
ESP021 Esophageal Cancer 84 0.505
35
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.505
36
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.505
37
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.505
38
P LNG021 Lung Occult Small Cell Carcinoma 20 0.505
39
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.496
40
PLY024 Polymicrogyria 46 0.496
41
P CRB045 Cerebellar Hypoplasia 40 0.464
42
MCR099 Microlissencephaly 39 0.429
44
ART140 Arteries, Anomalies of 52 0.304
45
LPP008 Lipoprotein Quantitative Trait Locus 65 0.304
46
CRP032 Corpus Callosum, Agenesis of 49 0.304
47
c LSS009 Lissencephaly 3 39 0.304
48
c SML038 Small Cell Cancer of the Lung 69 0.248
49
P LSS024 Lissencephaly with Cerebellar Hypoplasia 36 0.248
50
SPS057 Spasticity 43 0.248
51
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.175
52
MYL069 Myeloma, Multiple 77 0.175
53
ZTT001 Zttk Syndrome 36 0.175
54
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.175
55
P MDL005 Medulloblastoma 75 0.175
56
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 54 0.175
57
P EPL164 Epilepsy 70 0.175
58
GLB002 Glioblastoma 67 0.175
59
P MGL013 Megalencephaly 46 0.175
60
NRN016 Neuronal Migration Disorders 40 0.175
61
HMM003 Hemimegalencephaly 53 0.175
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