Search results for "[genes] MT-TK"

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

# Family MCID Name MIFTS Score
1
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 40 17.905
2
P LGH007 Leigh Syndrome 70 12.661
3
KRN002 Kearns-Sayre Syndrome 59 12.661
4
c CHR095 Chronic Progressive External Ophthalmoplegia 45 12.661
5
P MTC004 Mitochondrial Encephalomyopathy 40 12.661
6
MRR006 Merrf/melas Overlap Syndrome 14 12.661
7
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 10.337
8
c EPL070 Epilepsy, Progressive Myoclonic 2b 53 10.337
9
LBR030 Leber Optic Atrophy 52 10.337
10
P MTC069 Mitochondrial Disorders 52 10.337
11
ERL001 Early Myoclonic Encephalopathy 50 10.337
12
c EPL121 Epilepsy, Progressive Myoclonic 1a 42 10.337
13
UNV001 Unverricht-Lundborg Syndrome 40 10.337
14
PRL008 Paralytic Ileus 39 10.337
15
OCL011 Ocular Motility Disease 38 10.337
16
MTC005 Mitochondrial Metabolism Disease 38 10.337
17
PRS023 Pearson Syndrome 36 10.337
18
MLT002 Multiple Symmetrical Lipomatosis 36 10.337
19
DBT090 Diabetes and Deafness, Maternally Inherited 33 10.337
20
LPM010 Lipomatosis, Multiple Symmetric 29 10.337
21
CRB014 Cerebral Angioma 26 10.337
22
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.337
23
BRN027 Brain Angioma 21 10.337
24
MYC001 Myoclonic Cerebellar Dyssynergia 21 10.337
25
NNT041 Neonatal Period Electroclinical Syndrome 20 10.337
26
P MYP108 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 16 10.337
27
INT077 Intracranial Structure Hemangioma 14 10.337
28
CRN031 Cranial Nerve Disease 40 7.310
29
MSC004 Muscle Tissue Disease 36 7.310
30
MTC061 Mitochondrial Dna Depletion Syndrome 1 32 7.310
31
DBT019 Diabetes and Hearing Loss 16 7.310
32
MTR049 Maternally-Inherited Cardiomyopathy and Hearing Loss 12 7.310
33
c MTT006 Mt-Tt Related Parkinson Disease Susceptibility 8 7.310
34
c MLS007 Melas, Mt-Tk-Related 3 7.310