62 hits were found for 'MT-ATP6'

# Family MCID Name MIFTS Score
1
LBR002 Leber Hereditary Optic Neuropathy 63 3.927
2
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 28 3.635
3
DMN002 Dementia 66 2.968
4
ECH003 Echinococcosis 63 2.968
5
RTN023 Retinitis 61 2.968
6
KRN002 Kearns-Sayre Syndrome 59 2.968
7
P RNL007 Renal Tubular Acidosis 58 2.968
8
CYS008 Cystic Echinococcosis 57 2.968
9
c EPS003 Episodic Ataxia 55 2.968
10
HMP005 Hemiplegia 54 2.968
11
MTC069 Mitochondrial Disorders 47 2.968
12
c ATX004 Ataxia 38 2.968
13
MTR017 Maternally Inherited Leigh Syndrome 20 2.968
14
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 5 2.968
15
FML050 Familial Bilateral Striatal Necrosis 3 2.968
16
P PRK002 Parkinson's Disease 92 2.571
17
P RTN008 Retinitis Pigmentosa 81 2.571
18
P LGH001 Leigh Disease 67 2.571
19
NRP001 Neuropathy 61 2.571
20
STR038 Striatonigral Degeneration Infantile 25 2.571
21
MTR059 Maternally-Inherited Spastic Paraplegia 5 2.571
22
P PRS040 Prostate Cancer 91 2.142
23
PRS047 Prostatitis 62 2.142
24
TTH006 Tooth Disease 55 2.142
25
P ALZ001 Alzheimer's Disease 103 2.099
26
P OBS005 Obesity 93 2.099
27
P SYS001 Systemic Lupus Erythematosus 87 2.099
28
P HNT001 Huntington's Disease 87 2.099
29
P MLT020 Multiple Sclerosis 82 2.099
30
c HPT021 Hepatitis 75 2.099
31
c LPS004 Lupus Erythematosus 73 2.099
32
P CLR023 Colorectal Cancer 73 2.099
33
P FNC001 Fanconi's Anemia 67 2.099
34
DWN001 Down Syndrome 62 2.099
35
HRD010 Hereditary Spastic Paraplegia 59 2.099
36
P GLC007 Glaucoma 58 2.099
37
P MYP004 Myopathy 58 2.099
38
SNS001 Sensorineural Hearing Loss 56 2.099
39
c OPN001 Open-Angle Glaucoma 56 2.099
40
LPM005 Lipomatosis 52 2.099
41
c SPN049 Spinocerebellar Ataxia 51 2.099
42
PRP016 Paraplegia 48 2.099
43
MTC004 Mitochondrial Encephalomyopathy 43 2.099
44
STR001 Striatonigral Degeneration 43 2.099
45
MLT012 Multiple Symmetric Lipomatosis 43 2.099
46
MLT002 Multiple Symmetrical Lipomatosis 35 2.099
47
ENC011 Encephalomyopathy 29 2.099
48
SPS057 Spasticity 29 2.099
49
CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 2.099
50
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 4 2.099
51
NRP003 Neuropathy Ataxia Retinitis Pigmentosa Syndrome 26 1.583
52
c CHR071 Charcot-Marie-Tooth Disease 69 1.540
53
P MLT019 Multiple Myeloma 89 1.484
54
P HYP075 Hypertension 86 1.484
55
P OST018 Osteosarcoma 81 1.484
56
P PNM007 Pneumonia 79 1.484
57
P MLR004 Malaria 73 1.484
58
c ESS002 Essential Hypertension 71 1.484
59
P PLY019 Polyneuropathy 64 1.484
60
c MYL007 Myeloma 59 1.484
61
LCT001 Lactic Acidosis 49 1.484
62
HRD088 Hereditary Neuropathies 31 1.484