63 hits were found for 'MT-ATP6'

# ++ Fam MCID Name MIFTS Score
1
P LBR002 Leber Hereditary Optic Neuropathy 59 3.929
2
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 3.637
3
P DMN002 Dementia 61 2.970
4
RNL007 Renal Tubular Acidosis 57 2.970
5
c ATX004 Ataxia 56 2.970
6
KRN002 Kearns-Sayre Syndrome 53 2.970
7
RTN023 Retinitis 53 2.970
8
ECH003 Echinococcosis 52 2.970
9
c EPS003 Episodic Ataxia 50 2.970
10
CYS008 Cystic Echinococcosis 50 2.970
11
HMP005 Hemiplegia 47 2.970
12
P MTC069 Mitochondrial Disorders 46 2.970
13
MTR017 Maternally Inherited Leigh Syndrome 21 2.970
14
FML050 Familial Bilateral Striatal Necrosis 4 2.970
15
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 4 2.970
16
P PRK002 Parkinson's Disease 86 2.572
17
P RTN008 Retinitis Pigmentosa 76 2.572
18
P LGH001 Leigh Disease 56 2.572
19
NRP001 Neuropathy 54 2.572
20
STR038 Striatonigral Degeneration Infantile 16 2.572
21
MTR059 Maternally-Inherited Spastic Paraplegia 3 2.572
22
P PRS040 Prostate Cancer 76 2.143
23
TTH006 Tooth Disease 54 2.143
24
P ALZ001 Alzheimer's Disease 93 2.100
25
P SYS001 Systemic Lupus Erythematosus 83 2.100
26
P HNT001 Huntington's Disease 81 2.100
27
P OBS005 Obesity 79 2.100
28
P MLT020 Multiple Sclerosis 75 2.100
29
P CLR023 Colorectal Cancer 66 2.100
30
FNC001 Fanconi's Anemia 66 2.100
31
c LPS004 Lupus Erythematosus 65 2.100
32
c HPT021 Hepatitis 65 2.100
33
DWN001 Down Syndrome 58 2.100
34
SNS001 Sensorineural Hearing Loss 55 2.100
35
HRD010 Hereditary Spastic Paraplegia 54 2.100
36
c MYP004 Myopathy 52 2.100
37
c SPN049 Spinocerebellar Ataxia 51 2.100
38
P OPN001 Open-Angle Glaucoma 51 2.100
39
PRS047 Prostatitis 50 2.100
40
P GLC007 Glaucoma 49 2.100
41
LPM005 Lipomatosis 45 2.100
42
SPS057 Spasticity 42 2.100
43
PRP016 Paraplegia 42 2.100
44
ENC011 Encephalomyopathy 41 2.100
45
MLT012 Multiple Symmetric Lipomatosis 41 2.100
46
STR001 Striatonigral Degeneration 41 2.100
47
MTC004 Mitochondrial Encephalomyopathy 38 2.100
48
MLT002 Multiple Symmetrical Lipomatosis 29 2.100
49
CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 20 2.100
50
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 4 2.100
51
NRP003 Neuropathy Ataxia Retinitis Pigmentosa Syndrome 19 1.583
52
P CHR071 Charcot-Marie-Tooth Disease 61 1.541
53
P HYP075 Hypertension 76 1.485
54
P MLT019 Multiple Myeloma 76 1.485
55
P OST018 Osteosarcoma 70 1.485
56
P PNM007 Pneumonia 67 1.485
57
P MLR004 Malaria 66 1.485
58
c ESS002 Essential Hypertension 64 1.485
59
P PLY019 Polyneuropathy 54 1.485
60
c MYL007 Myeloma 53 1.485
61
LCT001 Lactic Acidosis 44 1.485
62
HRD088 Hereditary Neuropathies 35 1.485
63
NSY001 N Syndrome 57 0.067