Search results for "[genes] MT-TK"

35 hits were found for '[genes] MT-TK'

# Family MCID Name MIFTS Score
1
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 42 17.842
2
P LGH007 Leigh Syndrome 70 12.616
3
KRN002 Kearns-Sayre Syndrome 60 12.616
4
c CHR095 Chronic Progressive External Ophthalmoplegia 48 12.616
5
P MTC004 Mitochondrial Encephalomyopathy 39 12.616
6
c EPL070 Epilepsy, Progressive Myoclonic 2b 53 10.301
7
UNV001 Unverricht-Lundborg Syndrome 41 10.301
8
DBT090 Diabetes and Deafness, Maternally Inherited 32 10.301
9
ERL001 Early Myoclonic Encephalopathy 46 10.301
10
c GNG001 Gangliosidosis Gm1 56 10.301
11
ADP001 Adiposis Dolorosa 44 10.301
12
P MTC069 Mitochondrial Disorders 51 10.301
13
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 10.301
14
OCL011 Ocular Motility Disease 41 10.301
15
OPT006 Optic Nerve Disease 47 10.301
16
LPM010 Lipomatosis, Multiple Symmetric 27 10.301
17
MYC001 Myoclonic Cerebellar Dyssynergia 23 10.301
18
PRS023 Pearson Syndrome 37 10.301
19
GLY031 Glycoproteinosis 28 10.301
20
MTC005 Mitochondrial Metabolism Disease 37 10.301
21
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.301
22
PRL008 Paralytic Ileus 37 10.301
23
INT077 Intracranial Structure Hemangioma 13 10.301
24
CRB014 Cerebral Angioma 25 10.301
25
MLT002 Multiple Symmetrical Lipomatosis 36 10.301
26
MRR006 Merrf/melas Overlap Syndrome 14 10.301
27
BRN027 Brain Angioma 20 10.301
28
NNT041 Neonatal Period Electroclinical Syndrome 19 10.301
29
P MYP108 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 17 10.301
30
MTC061 Mitochondrial Dna Depletion Syndrome 1 31 7.284
31
CRN031 Cranial Nerve Disease 39 7.284
32
MTR049 Maternally-Inherited Cardiomyopathy and Hearing Loss 6 7.284
33
c MTT006 Mt-Tt Related Parkinson Disease Susceptibility 8 7.284
34
c MLS007 Melas, Mt-Tk-Related 3 7.284
35
MSC004 Muscle Tissue Disease 35 7.284