Search results for "MT-ATP6"

28 hits were found for 'MT-ATP6'

# Family MCID Name MIFTS Score
1
LBR002 Leber Hereditary Optic Neuropathy 64 5.300
2
LGH009 Leigh Syndrome Due to Mitochondrial Complex I Deficiency 31 4.958
3
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 30 4.590
4
P LGH001 Leigh Disease 69 4.190
5
DMN002 Dementia 66 3.748
6
P MTC069 Mitochondrial Disorders 53 3.748
7
LGH015 Leigh Syndrome Due to Mitochondrial Cox4 Deficiency 28 3.748
8
LGH010 Leigh Syndrome, Due to Cox Deficiency 27 3.748
9
LGH002 Leigh Syndrome Due to Cytochrome C Oxidase Deficiency 27 3.748
10
NRP003 Neuropathy Ataxia Retinitis Pigmentosa Syndrome 30 3.329
11
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 8 3.246
12
P RTN008 Retinitis Pigmentosa 86 2.650
13
CYS008 Cystic Echinococcosis 73 2.650
14
KRN002 Kearns-Sayre Syndrome 63 2.650
15
RNL007 Renal Tubular Acidosis 56 2.650
16
HRD088 Hereditary Neuropathies 32 2.650
17
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 25 2.650
18
VSL005 Visual Pathway Disease 21 2.650
19
MTC021 Mitochondrial Complex V Deficiency 18 2.650
20
FML050 Familial Bilateral Striatal Necrosis 5 2.650
21
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 4 2.650
22
STR038 Striatonigral Degeneration Infantile 26 1.874
23
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 9 1.874
24
MTR059 Maternally-Inherited Spastic Paraplegia 5 1.874
25
P PRS040 Prostate Cancer 97 0.082
26
P CHR071 Charcot-Marie-Tooth Disease 73 0.082
27
PRS047 Prostatitis 59 0.082
28
TTH006 Tooth Disease 55 0.082