Search results for "[genes] C10orf2"

24 hits were found for '[genes] C10orf2'

# Family MCID Name MIFTS Score
1
MTC054 Mitochondrial Dna Depletion Syndrome 7 36 21.735
2
c PRR026 Perrault Syndrome 5 18 20.331
3
P OPH004 Ophthalmoplegia 51 18.823
4
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 34 18.823
5
P PRR025 Perrault Syndrome 40 17.183
6
c CHR095 Chronic Progressive External Ophthalmoplegia 45 15.369
7
P MTC069 Mitochondrial Disorders 52 13.310
8
DBT004 Diabetic Polyneuropathy 50 13.310
9
MTC057 Mitochondrial Recessive Ataxia Syndrome 42 13.310
10
P AXN001 Axonal Neuropathy 38 13.310
11
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 36 13.310
12
P MLS001 Melas Syndrome 59 10.868
13
BLL001 Baller-Gerold Syndrome 52 10.868
14
c SPN304 Spinocerebellar Ataxia 8 44 10.868
15
MTC056 Mitochondrial Dna Depletion Syndrome 4a 43 10.868
16
MRR001 Merrf Syndrome 43 10.868
17
OCL011 Ocular Motility Disease 42 10.868
18
ATH004 Athetosis 22 10.868
19
PLG003 Polg-Related Disorders 15 10.868
20
P ATX010 Ataxia Neuropathy Spectrum 34 7.685
21
MTC063 Mitochondrial Dna Depletion Syndrome 3 24 7.685
22
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 8 7.685
23
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 5 7.685
24
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 5 7.685