Search results for "[genes] MT-TL1"

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

# Family MCID Name MIFTS Score
1
MTR046 Maternally Inherited Diabetes and Deafness 40 15.072
2
MRR006 Merrf/melas Overlap Syndrome 15 13.053
3
P MLS001 Melas Syndrome 59 10.658
4
KRN002 Kearns-Sayre Syndrome 53 10.658
5
P MTC069 Mitochondrial Disorders 52 10.658
6
MRR001 Merrf Syndrome 43 10.658
7
DBT019 Diabetes and Hearing Loss 17 10.658
8
c MCL042 Macular Degeneration, Age-Related, 1 73 7.536
9
MYL009 Myelodysplastic Syndrome 72 7.536
10
P LGH007 Leigh Syndrome 71 7.536
11
P SDD001 Sudden Infant Death Syndrome 59 7.536
12
MTC097 Mitochondrial Complex Iv Deficiency 50 7.536
13
CYC008 Cyclic Vomiting Syndrome 42 7.536
14
c 3MT015 3-Methylglutaconic Aciduria, Type I 37 7.536
15
c PRG104 Progressive External Ophthalmoplegia, Autosomal Recessive 1 36 7.536
16
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 34 7.536
17
MTC028 Mitochondrial Cardiomyopathy 32 7.536
18
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 32 7.536
19
c PRG105 Progressive External Ophthalmoplegia, Autosomal Dominant 1 32 7.536
20
c MCL043 Macular Degeneration, Age-Related, 2 31 7.536
21
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 30 7.536
22
P 3MT007 3-Methylglutaconic Aciduria 30 7.536
23
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 29 7.536
24
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 22 7.536
25
MTR058 Maternally-Inherited Progressive External Ophthalmoplegia 15 7.536
26
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 12 7.536
27
c MLS008 Melas, Mt-Tl1-Related 8 7.536
28
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 6 7.536