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 39 18.241
2
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 16.651
3
P LGH007 Leigh Syndrome 70 14.893
4
KRN002 Kearns-Sayre Syndrome 61 14.893
5
P LCT001 Lactic Acidosis 51 14.893
6
c INT072 Intestinal Pseudo-Obstruction 46 14.893
7
P MTC004 Mitochondrial Encephalomyopathy 42 14.893
8
DBT090 Diabetes and Deafness, Maternally Inherited 33 14.893
9
DBT019 Diabetes and Hearing Loss 15 14.893
10
MRR006 Merrf/melas Overlap Syndrome 14 14.893
11
P SDD001 Sudden Infant Death Syndrome 61 12.898
12
P MTC069 Mitochondrial Disorders 53 12.898
13
c 3MT015 3-Methylglutaconic Aciduria, Type I 40 12.898
14
P 3MT007 3-Methylglutaconic Aciduria 39 12.898
15
CYC008 Cyclic Vomiting Syndrome 37 12.898
16
c MCL043 Macular Degeneration, Age-Related, 2 32 12.898
17
MTC028 Mitochondrial Cardiomyopathy 32 12.898
18
DPH003 Diphyllobothriasis 28 12.898
19
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 12.898
20
MTR058 Maternally-Inherited Progressive External Ophthalmoplegia 14 12.898
21
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 9 12.898
22
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 6 12.898
23
c MLS008 Melas, Mt-Tl1-Related 3 12.898
24
MYL009 Myelodysplastic Syndrome 73 10.531
25
MTC097 Mitochondrial Complex Iv Deficiency 51 10.531
26
c PRG104 Progressive External Ophthalmoplegia, Autosomal Recessive 1 35 10.531
27
c PRG105 Progressive External Ophthalmoplegia, Autosomal Dominant 1 32 10.531
28
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 30 10.531
29
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 27 10.531
30
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 27 10.531