50 hits were found for 'C10orf2'
Try searching for c19orf12

# Family MCID Name MIFTS Score
1
c OPH004 Ophthalmoplegia 52 5.115
2
MTC054 Mitochondrial Dna Depletion Syndrome 7 28 5.014
3
c SPN049 Spinocerebellar Ataxia 51 4.509
4
INF010 Infantile Onset Spinocerebellar Ataxia 39 4.509
5
c PRG049 Progressive External Ophthalmoplegia, Autosomal Dominant, 3 15 4.509
6
P ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 43 3.938
7
c ATX004 Ataxia 38 3.545
8
P CHR095 Chronic Progressive External Ophthalmoplegia 50 3.205
9
DBT004 Diabetic Polyneuropathy 57 3.171
10
HRD026 Hereditary Ataxia 48 3.171
11
P ATX010 Ataxia Neuropathy Spectrum 44 3.171
12
MTC010 Mitochondrial Dna Depletion Syndrome 35 3.171
13
WSR001 Was-Related Disorders 28 3.171
14
MTC034 Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 15 3.171
15
PLG003 Polg-Related Disorders 14 3.171
16
NRP001 Neuropathy 61 2.785
17
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 8 2.746
18
P ALZ001 Alzheimer's Disease 103 2.242
19
c DBT009 Diabetes Mellitus 80 2.242
20
c TYP008 Type 1 Diabetes Mellitus 77 2.242
21
CHL065 Cholangiocarcinoma 73 2.242
22
P TYP020 Type 1 Diabetes 69 2.242
23
ALP003 Alpers Syndrome 66 2.242
24
DMN002 Dementia 66 2.242
25
CRB042 Cerebellar Ataxia 66 2.242
26
P PLY019 Polyneuropathy 64 2.242
27
PRS047 Prostatitis 62 2.242
28
DNT005 Dentatorubral-Pallidoluysian Atrophy 61 2.242
29
P MYP004 Myopathy 58 2.242
30
MRR001 Merrf Syndrome 52 2.242
31
MTC069 Mitochondrial Disorders 47 2.242
32
INT079 Intrahepatic Cholangiocarcinoma 43 2.242
33
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 20 2.242
34
DGK001 Dguok-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 18 2.242
35
ATH004 Athetosis 16 2.242
36
P MLT019 Multiple Myeloma 89 1.586
37
MLT021 Multiple System Atrophy 76 1.586
38
P MLR004 Malaria 73 1.586
39
P HYP080 Hypogonadism 60 1.586
40
c MYL007 Myeloma 59 1.586
41
c CTR002 Cataract 53 1.586
42
PRP023 Peripheral Neuropathy 53 1.586
43
c OPT004 Optic Atrophy 46 1.586
44
AXN001 Axonal Neuropathy 45 1.586
45
HYP265 Hypotonia 30 1.586
46
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 9 1.586
47
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 8 1.586
48
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 4 1.586
49
MTC061 Mitochondrial Dna Depletion Syndrome 1 35 0.071
50
PRG050 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions 3 11 0.071