Search results for "[genes] MT-TK"

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

# Family MCID Name MIFTS Score
1
MRR001 Merrf Syndrome 48 16.693
2
c CHR095 Chronic Progressive External Ophthalmoplegia 42 12.930
3
P MTC004 Mitochondrial Encephalomyopathy 32 12.930
4
MRR006 Merrf/melas Overlap Syndrome 15 12.930
5
P LGH007 Leigh Syndrome 67 10.557
6
KRN002 Kearns-Sayre Syndrome 53 10.557
7
P MLS001 Melas Syndrome 53 10.557
8
c EPL070 Epilepsy, Progressive Myoclonic 2b 52 10.557
9
P MTC069 Mitochondrial Disorders 49 10.557
10
ERL001 Early Myoclonic Encephalopathy 44 10.557
11
MTR046 Maternally Inherited Diabetes and Deafness 43 10.557
12
PRS023 Pearson Syndrome 43 10.557
13
MLT012 Multiple Symmetric Lipomatosis 40 10.557
14
UNV001 Unverricht-Lundborg Syndrome 37 10.557
15
MLT002 Multiple Symmetrical Lipomatosis 34 10.557
16
PRL008 Paralytic Ileus 33 10.557
17
OCL011 Ocular Motility Disease 26 10.557
18
MYC001 Myoclonic Cerebellar Dyssynergia 22 10.557
19
NNT041 Neonatal Period Electroclinical Syndrome 18 10.557
20
CRB014 Cerebral Angioma 16 10.557
21
BRN027 Brain Angioma 11 10.557
22
INT077 Intracranial Structure Hemangioma 11 10.557
23
c PRK057 Parkinson Disease, Late-Onset 73 7.465
24
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 32 7.465
25
MTR017 Maternally Inherited Leigh Syndrome 30 7.465
26
MTC061 Mitochondrial Dna Depletion Syndrome 1 28 7.465
27
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 7.465
28
DBT019 Diabetes and Hearing Loss 11 7.465
29
c MLS007 Melas, Mt-Tk-Related 8 7.465
30
MTR049 Maternally-Inherited Cardiomyopathy and Hearing Loss 7 7.465