Search results for "[genes] MT-ATP6"

31 hits were found for '[genes] MT-ATP6'

# Family MCID Name MIFTS Score
1
P LGH007 Leigh Syndrome 67 23.507
2
LBR002 Leber Hereditary Optic Neuropathy 58 22.300
3
P MTC069 Mitochondrial Disorders 49 18.208
4
P RTN008 Retinitis Pigmentosa 75 16.622
5
P NRP001 Neuropathy 48 16.622
6
P ATX004 Ataxia 43 16.622
7
P LCT001 Lactic Acidosis 40 16.622
8
P SDR003 Sideroblastic Anemia 38 16.622
9
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 14 16.622
10
c MYP107 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 12 16.622
11
MTC005 Mitochondrial Metabolism Disease 26 14.867
12
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 16 14.867
13
P CRD011 Cardiomyopathy 53 12.875
14
KRN002 Kearns-Sayre Syndrome 53 12.875
15
ECH003 Echinococcosis 51 12.875
16
CYS008 Cystic Echinococcosis 51 12.875
17
OPT006 Optic Nerve Disease 39 12.875
18
CRN031 Cranial Nerve Disease 30 12.875
19
MTR017 Maternally Inherited Leigh Syndrome 30 12.875
20
NRP003 Neuropathy Ataxia Retinitis Pigmentosa Syndrome 29 12.875
21
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 12.875
22
MTC021 Mitochondrial Complex V Deficiency 13 12.875
23
P CHR071 Charcot-Marie-Tooth Disease 59 10.513
24
P MLS001 Melas Syndrome 53 10.513
25
LFT009 Left Ventricular Outflow Tract Obstruction 41 10.513
26
P FML050 Familial Bilateral Striatal Necrosis 6 10.513
27
MTC064 Mitochondrial Myopathy and Sideroblastic Anemia 1 38 7.433
28
LBR030 Leber Optic Atrophy 24 7.433
29
c FML309 Familial Infantile Bilateral Striatal Necrosis 15 7.433
30
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 14 7.433
31
MTR059 Maternally-Inherited Spastic Paraplegia 6 7.433