Search results for "C10orf2"

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

# Family MCID Name MIFTS Score
1
c PRG049 Progressive External Ophthalmoplegia, Autosomal Dominant, 3 16 17.889
2
c OPH004 Ophthalmoplegia 53 5.583
3
c ATX004 Ataxia 59 5.509
4
c SPN049 Spinocerebellar Ataxia 56 5.509
5
INF010 Infantile Onset Spinocerebellar Ataxia 43 4.786
6
MTC054 Mitochondrial Dna Depletion Syndrome 7 26 4.723
7
P ATX010 Ataxia Neuropathy Spectrum 43 4.311
8
P CHR095 Chronic Progressive External Ophthalmoplegia 56 3.896
9
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 47 3.492
10
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 24 3.340
11
ALP003 Alpers Syndrome 61 2.727
12
c HRD026 Hereditary Ataxia 53 2.727
13
DBT004 Diabetic Polyneuropathy 52 2.727
14
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 2.727
15
PLG003 Polg-Related Disorders 15 2.727
16
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 9 2.727
17
P MTC069 Mitochondrial Disorders 50 1.928
18
MTC063 Mitochondrial Dna Depletion Syndrome 3 17 1.928
19
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 9 1.928
20
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 7 1.928
21
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 5 1.928
22
P MYP004 Myopathy 62 0.083
23
NRP001 Neuropathy 62 0.083
24
P PLY019 Polyneuropathy 61 0.083
25
MTC061 Mitochondrial Dna Depletion Syndrome 1 19 0.083
26
PRG050 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions 3 12 0.083