Search results for "C10orf2"

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

# Family MCID Name MIFTS Score
1
c PRG049 Progressive External Ophthalmoplegia, Autosomal Dominant, 3 16 17.795
2
c OPH004 Ophthalmoplegia 53 5.589
3
c ATX004 Ataxia 58 5.486
4
c SPN049 Spinocerebellar Ataxia 56 5.486
5
INF010 Infantile Onset Spinocerebellar Ataxia 41 4.759
6
MTC054 Mitochondrial Dna Depletion Syndrome 7 26 4.314
7
P CHR095 Chronic Progressive External Ophthalmoplegia 55 3.898
8
MTC010 Mitochondrial Dna Depletion Syndrome 42 3.858
9
P ATX010 Ataxia Neuropathy Spectrum 41 3.858
10
P ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 47 3.497
11
ALP003 Alpers Syndrome 60 2.728
12
c HRD026 Hereditary Ataxia 53 2.728
13
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 2.728
14
DBT004 Diabetic Polyneuropathy 45 2.728
15
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 24 2.728
16
PLG003 Polg-Related Disorders 15 2.728
17
P MTC069 Mitochondrial Disorders 50 1.929
18
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 10 1.929
19
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 8 1.929
20
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 7 1.929
21
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 5 1.929
22
NRP001 Neuropathy 61 0.085
23
MTC061 Mitochondrial Dna Depletion Syndrome 1 35 0.085
24
PRG050 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions 3 12 0.085