Search results for "[genes] C10orf2"

24 hits were found for '[genes] C10orf2'

# Family MCID Name MIFTS Score
1
MTC054 Mitochondrial Dna Depletion Syndrome 7 38 21.735
2
c PRR026 Perrault Syndrome 5 35 20.331
3
P OPH004 Ophthalmoplegia 42 18.823
4
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 37 18.823
5
P PRR025 Perrault Syndrome 43 17.183
6
c CHR095 Chronic Progressive External Ophthalmoplegia 42 15.369
7
P MTC069 Mitochondrial Disorders 48 13.310
8
DBT004 Diabetic Polyneuropathy 45 13.310
9
MTC057 Mitochondrial Recessive Ataxia Syndrome 39 13.310
10
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 33 13.310
11
P AXN001 Axonal Neuropathy 32 13.310
12
BLL001 Baller-Gerold Syndrome 53 10.868
13
P MLS001 Melas Syndrome 50 10.868
14
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 10.868
15
MRR001 Merrf Syndrome 43 10.868
16
c SPN304 Spinocerebellar Ataxia 8 40 10.868
17
OCL011 Ocular Motility Disease 27 10.868
18
ATH004 Athetosis 21 10.868
19
PLG003 Polg-Related Disorders 17 10.868
20
MTC063 Mitochondrial Dna Depletion Syndrome 3 28 7.685
21
P ATX010 Ataxia Neuropathy Spectrum 19 7.685
22
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 7 7.685
23
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 4 7.685
24
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 3 7.685