Search results for "[genes] MT-TL1"

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

# Family MCID Name MIFTS Score
1
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 40 16.616
2
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 14.862
3
P LGH007 Leigh Syndrome 70 12.871
4
KRN002 Kearns-Sayre Syndrome 59 12.871
5
c INT072 Intestinal Pseudo-Obstruction 46 12.871
6
P MTC004 Mitochondrial Encephalomyopathy 40 12.871
7
MRR006 Merrf/melas Overlap Syndrome 14 12.871
8
P MTC069 Mitochondrial Disorders 52 10.509
9
DBT090 Diabetes and Deafness, Maternally Inherited 33 10.509
10
DPH003 Diphyllobothriasis 27 10.509
11
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.509
12
DBT019 Diabetes and Hearing Loss 16 10.509
13
MYL009 Myelodysplastic Syndrome 74 7.431
14
c MCL042 Macular Degeneration, Age-Related, 1 71 7.431
15
P SDD001 Sudden Infant Death Syndrome 61 7.431
16
MTC097 Mitochondrial Complex Iv Deficiency 51 7.431
17
c 3MT015 3-Methylglutaconic Aciduria, Type I 39 7.431
18
CYC008 Cyclic Vomiting Syndrome 38 7.431
19
P 3MT007 3-Methylglutaconic Aciduria 38 7.431
20
c PRG104 Progressive External Ophthalmoplegia, Autosomal Recessive 1 38 7.431
21
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 34 7.431
22
c PRG105 Progressive External Ophthalmoplegia, Autosomal Dominant 1 34 7.431
23
c MCL043 Macular Degeneration, Age-Related, 2 34 7.431
24
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 31 7.431
25
MTC028 Mitochondrial Cardiomyopathy 30 7.431
26
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 30 7.431
27
MTR058 Maternally-Inherited Progressive External Ophthalmoplegia 14 7.431
28
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 10 7.431
29
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 6 7.431
30
c MLS008 Melas, Mt-Tl1-Related 3 7.431