Search results for "MT-ATP6"

27 hits were found for 'MT-ATP6'

# Family MCID Name MIFTS Score
1
LBR002 Leber Hereditary Optic Neuropathy 60 4.628
2
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 31 4.628
3
LGH009 Leigh Syndrome Due to Mitochondrial Complex I Deficiency 30 4.628
4
DMN002 Dementia 66 3.779
5
P LGH001 Leigh Disease 64 3.779
6
P MTC069 Mitochondrial Disorders 50 3.779
7
LGH010 Leigh Syndrome, Due to Cox Deficiency 27 3.273
8
LGH002 Leigh Syndrome Due to Cytochrome C Oxidase Deficiency 27 3.273
9
LGH015 Leigh Syndrome Due to Mitochondrial Cox4 Deficiency 27 3.273
10
NRP003 Neuropathy Ataxia Retinitis Pigmentosa Syndrome 25 2.769
11
CYS008 Cystic Echinococcosis 64 2.672
12
KRN002 Kearns-Sayre Syndrome 61 2.672
13
P RNL007 Renal Tubular Acidosis 57 2.672
14
HRD088 Hereditary Neuropathies 32 2.672
15
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 25 2.672
16
VSL005 Visual Pathway Disease 20 2.672
17
MTC021 Mitochondrial Complex V Deficiency 18 2.672
18
FML050 Familial Bilateral Striatal Necrosis 5 2.672
19
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 5 2.672
20
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 4 2.672
21
STR038 Striatonigral Degeneration Infantile 23 1.889
22
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 9 1.889
23
MTR059 Maternally-Inherited Spastic Paraplegia 5 1.889
24
P PRS040 Prostate Cancer 87 0.083
25
P CHR071 Charcot-Marie-Tooth Disease 70 0.083
26
PRS047 Prostatitis 60 0.083
27
TTH006 Tooth Disease 55 0.083