35 hits were found for 'MT-TL1'

# Family MCID Name MIFTS Score
1
MTC069 Mitochondrial Disorders 47 4.206
2
SNS001 Sensorineural Hearing Loss 56 3.434
3
LCT001 Lactic Acidosis 49 3.434
4
MTC004 Mitochondrial Encephalomyopathy 43 3.434
5
ENC011 Encephalomyopathy 29 3.434
6
MRR006 Merrf/melas Overlap Syndrome 9 3.434
7
P MLS001 Melas Syndrome 61 3.016
8
MTR046 Maternally Inherited Diabetes and Deafness 45 3.016
9
KRN002 Kearns-Sayre Syndrome 59 2.974
10
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 28 2.974
11
MTC028 Mitochondrial Cardiomyopathy 21 2.974
12
MTR058 Maternally-Inherited Progressive External Ophthalmoplegia 17 2.974
13
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 4 2.974
14
DBT019 Diabetes and Hearing Loss 3 2.974
15
c MLS008 Melas, Mt-Tl1-Related 2 2.974
16
P HYP075 Hypertension 86 2.428
17
P MLT020 Multiple Sclerosis 82 2.428
18
c DBT009 Diabetes Mellitus 80 2.428
19
WRN001 Werner Syndrome 75 2.428
20
P LNG032 Lung Cancer 74 2.428
21
c ESS002 Essential Hypertension 71 2.428
22
P TYP020 Type 1 Diabetes 69 2.428
23
c PNC044 Pancreatitis 67 2.428
24
P PLY019 Polyneuropathy 64 2.428
25
c HYP061 Hypertrophic Cardiomyopathy 61 2.428
26
P MYP004 Myopathy 58 2.428
27
c SPN049 Spinocerebellar Ataxia 51 2.428
28
c ATX004 Ataxia 38 2.428
29
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 25 2.428
30
ATH003 Atherosclerosis 71 1.717
31
P LGH001 Leigh Disease 67 1.717
32
MRR001 Merrf Syndrome 52 1.717
33
c OPH004 Ophthalmoplegia 52 1.717
34
P CRN157 Coronary Heart Disease 43 1.717
35
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 6 1.717