Search results for "[genes] C10orf2"

23 hits were found for '[genes] C10orf2'

# Family MCID Name MIFTS Score
1
MTC054 Mitochondrial Dna Depletion Syndrome 7 43 23.164
2
P PRR025 Perrault Syndrome 44 21.839
3
c PRR026 Perrault Syndrome 5 18 20.428
4
P OPH004 Ophthalmoplegia 43 18.913
5
c CHR095 Chronic Progressive External Ophthalmoplegia 42 18.913
6
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 36 18.913
7
P MTC069 Mitochondrial Disorders 49 13.373
8
DBT004 Diabetic Polyneuropathy 46 13.373
9
MTC057 Mitochondrial Recessive Ataxia Syndrome 44 13.373
10
SPN050 Spinocerebellar Degeneration 35 13.373
11
P AXN001 Axonal Neuropathy 35 13.373
12
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 30 13.373
13
BLL001 Baller-Gerold Syndrome 54 10.919
14
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 10.919
15
MRR001 Merrf Syndrome 48 10.919
16
OCL011 Ocular Motility Disease 26 10.919
17
ATH004 Athetosis 24 10.919
18
PLG003 Polg-Related Disorders 15 10.919
19
P ATX010 Ataxia Neuropathy Spectrum 31 7.721
20
MTC063 Mitochondrial Dna Depletion Syndrome 3 26 7.721
21
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 8 7.721
22
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 7 7.721
23
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 5 7.721