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

# ++ Fam MCID Name MIFTS Score
1
c OPH004 Ophthalmoplegia 46 5.120
2
MTC054 Mitochondrial Dna Depletion Syndrome 7 19 5.018
3
c SPN049 Spinocerebellar Ataxia 51 4.513
4
INF010 Infantile Onset Spinocerebellar Ataxia 36 4.513
5
c PRG049 Progressive External Ophthalmoplegia, Autosomal Dominant, 3 6 4.513
6
P ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 38 4.011
7
c ATX004 Ataxia 56 3.579
8
P CHR095 Chronic Progressive External Ophthalmoplegia 46 3.208
9
DBT004 Diabetic Polyneuropathy 52 3.174
10
HRD026 Hereditary Ataxia 45 3.174
11
c ATX010 Ataxia Neuropathy Spectrum 33 3.174
12
MTC010 Mitochondrial Dna Depletion Syndrome 29 3.174
13
WSR001 Was-Related Disorders 22 3.174
14
PLG003 Polg-Related Disorders 11 3.174
15
MTC034 Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 10 3.174
16
NRP001 Neuropathy 54 2.787
17
C10001 C10orf2-Related Ataxia Neuropathy Spectrum Disorders 6 2.749
18
P ALZ001 Alzheimer's Disease 93 2.244
19
P TYP020 Type 1 Diabetes 73 2.244
20
c TYP008 Type 1 Diabetes Mellitus 71 2.244
21
c DBT009 Diabetes Mellitus 68 2.244
22
CHL065 Cholangiocarcinoma 61 2.244
23
P DMN002 Dementia 61 2.244
24
CRB042 Cerebellar Ataxia 57 2.244
25
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 2.244
26
ALP003 Alpers Syndrome 55 2.244
27
P PLY019 Polyneuropathy 54 2.244
28
c MYP004 Myopathy 52 2.244
29
PRS047 Prostatitis 50 2.244
30
MRR001 Merrf Syndrome 47 2.244
31
P MTC069 Mitochondrial Disorders 46 2.244
32
INT079 Intrahepatic Cholangiocarcinoma 34 2.244
33
ATH004 Athetosis 25 2.244
34
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 18 2.244
35
DGK001 Dguok-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 14 2.244
36
P MLT019 Multiple Myeloma 76 1.587
37
P MLR004 Malaria 66 1.587
38
P MLT021 Multiple System Atrophy 64 1.587
39
HYP080 Hypogonadism 54 1.587
40
c MYL007 Myeloma 53 1.587
41
c CTR002 Cataract 48 1.587
42
PRP023 Peripheral Neuropathy 46 1.587
43
AXN001 Axonal Neuropathy 44 1.587
44
HYP265 Hypotonia 43 1.587
45
c OPT004 Optic Atrophy 41 1.587
46
c PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 9 1.587
47
C10002 C10orf2-Related Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form 2 1.587
48
MTC094 Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form 2 1.587
49
MTC061 Mitochondrial Dna Depletion Syndrome 1 24 0.071
50
c PRG050 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions 3 6 0.071