Search results for "[genes] MT-TL1"

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

# Family MCID Name MIFTS Score
1
P MTC069 Mitochondrial Disorders 47 18.403
2
MTR046 Maternally Inherited Diabetes and Deafness 44 15.026
3
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 26 13.013
4
MRR006 Merrf/melas Overlap Syndrome 11 13.013
5
KRN002 Kearns-Sayre Syndrome 52 10.625
6
P MLS001 Melas Syndrome 50 10.625
7
SNS001 Sensorineural Hearing Loss 48 10.625
8
MRR001 Merrf Syndrome 48 10.625
9
P ENC011 Encephalomyopathy 42 10.625
10
P LCT001 Lactic Acidosis 42 10.625
11
P MTC004 Mitochondrial Encephalomyopathy 32 10.625
12
c MCL042 Macular Degeneration, Age-Related, 1 72 7.513
13
MYL009 Myelodysplastic Syndrome 67 7.513
14
P LGH007 Leigh Syndrome 65 7.513
15
P SDD001 Sudden Infant Death Syndrome 62 7.513
16
MTC097 Mitochondrial Complex Iv Deficiency 48 7.513
17
c CHR095 Chronic Progressive External Ophthalmoplegia 48 7.513
18
MTR017 Maternally Inherited Leigh Syndrome 42 7.513
19
c 3MT015 3-Methylglutaconic Aciduria, Type I 36 7.513
20
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 35 7.513
21
CYC008 Cyclic Vomiting Syndrome 28 7.513
22
MTC028 Mitochondrial Cardiomyopathy 28 7.513
23
c MCL043 Macular Degeneration, Age-Related, 2 17 7.513
24
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 6 7.513
25
c MLS008 Melas, Mt-Tl1-Related 5 7.513
26
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 4 7.513
27
DBT019 Diabetes and Hearing Loss 4 7.513