Search results for "[genes] C10orf2"

21 hits were found for '[genes] C10orf2'

# Family MCID Name MIFTS Score
1
MTC054 Mitochondrial Dna Depletion Syndrome 7 38 21.995
2
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 33 17.388
3
P PRR025 Perrault Syndrome 42 17.388
4
c PRR026 Perrault Syndrome 5 18 17.388
5
KRN002 Kearns-Sayre Syndrome 60 13.469
6
c CHR095 Chronic Progressive External Ophthalmoplegia 48 13.469
7
DBT004 Diabetic Polyneuropathy 49 13.469
8
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 31 13.469
9
P AXN001 Axonal Neuropathy 37 13.469
10
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 10.997
11
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 42 10.997
12
c SPN304 Spinocerebellar Ataxia 8 42 10.997
13
BLL001 Baller-Gerold Syndrome 52 10.997
14
P MTC069 Mitochondrial Disorders 51 10.997
15
OCL011 Ocular Motility Disease 41 10.997
16
ATH004 Athetosis 25 10.997
17
PLG003 Polg-Related Disorders 18 10.997
18
MTC057 Mitochondrial Recessive Ataxia Syndrome 48 7.776
19
MTC093 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 7 7.776
20
c C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 4 7.776
21
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 3 7.776