Search results for "[genes] MT-TL1"

25 hits were found for '[genes] MT-TL1'

# Family MCID Name MIFTS Score
1
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 42 17.015
2
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 15.218
3
P LGH007 Leigh Syndrome 70 13.180
4
KRN002 Kearns-Sayre Syndrome 60 13.180
5
c INT072 Intestinal Pseudo-Obstruction 45 13.180
6
P MTC004 Mitochondrial Encephalomyopathy 39 13.180
7
MRR006 Merrf/melas Overlap Syndrome 14 13.180
8
c CHR095 Chronic Progressive External Ophthalmoplegia 48 10.761
9
DBT090 Diabetes and Deafness, Maternally Inherited 32 10.761
10
P MTC069 Mitochondrial Disorders 51 10.761
11
DPH003 Diphyllobothriasis 28 10.761
12
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.761
13
DBT019 Diabetes and Hearing Loss 9 10.761
14
c MCL042 Macular Degeneration, Age-Related, 1 71 7.609
15
MTC097 Mitochondrial Complex Iv Deficiency 51 7.609
16
MYL009 Myelodysplastic Syndrome 73 7.609
17
P SDD001 Sudden Infant Death Syndrome 60 7.609
18
c 3MT015 3-Methylglutaconic Aciduria, Type I 35 7.609
19
c MCL043 Macular Degeneration, Age-Related, 2 32 7.609
20
CYC008 Cyclic Vomiting Syndrome 39 7.609
21
P 3MT007 3-Methylglutaconic Aciduria 37 7.609
22
MTC028 Mitochondrial Cardiomyopathy 29 7.609
23
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 5 7.609
24
c MLS008 Melas, Mt-Tl1-Related 3 7.609
25
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 9 7.609