37 hits were found for 'MT-TL1'

# ++ Fam MCID Name MIFTS Score
1
P MTC069 Mitochondrial Disorders 46 4.178
2
SNS001 Sensorineural Hearing Loss 55 3.411
3
LCT001 Lactic Acidosis 44 3.411
4
ENC011 Encephalomyopathy 41 3.411
5
MTC004 Mitochondrial Encephalomyopathy 38 3.411
6
MRR006 Merrf/melas Overlap Syndrome 12 3.411
7
P MLS001 Melas Syndrome 50 2.996
8
KRN002 Kearns-Sayre Syndrome 53 2.954
9
MTR046 Maternally Inherited Diabetes and Deafness 35 2.954
10
MTC028 Mitochondrial Cardiomyopathy 31 2.954
11
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 2.954
12
MTR058 Maternally-Inherited Progressive External Ophthalmoplegia 13 2.954
13
DBT019 Diabetes and Hearing Loss 2 2.954
14
c CRD048 Cardiomyopathy with or Without Skeletal Myopathy 1 2.954
15
c MLS008 Melas, Mt-Tl1-Related 1 2.954
16
P TYP009 Type 2 Diabetes Mellitus 80 2.412
17
P HYP075 Hypertension 76 2.412
18
P MLT020 Multiple Sclerosis 75 2.412
19
P TYP020 Type 1 Diabetes 73 2.412
20
c DBT009 Diabetes Mellitus 68 2.412
21
WRN001 Werner Syndrome 68 2.412
22
c ESS002 Essential Hypertension 64 2.412
23
LNG032 Lung Cancer 61 2.412
24
c HYP061 Hypertrophic Cardiomyopathy 59 2.412
25
c PNC044 Pancreatitis 58 2.412
26
c ATX004 Ataxia 56 2.412
27
P PLY019 Polyneuropathy 54 2.412
28
c MYP004 Myopathy 52 2.412
29
c SPN049 Spinocerebellar Ataxia 51 2.412
30
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 24 2.412
31
ATH003 Atherosclerosis 69 1.706
32
P CRN157 Coronary Heart Disease 59 1.706
33
P LGH001 Leigh Disease 56 1.706
34
MRR001 Merrf Syndrome 47 1.706
35
c OPH004 Ophthalmoplegia 46 1.706
36
HYP492 Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation 2 1.706
37
3MS001 3-M Syndrome 45 0.077