Search results for "[genes] MT-ATP6"

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

# Family MCID Name MIFTS Score
1
P LGH007 Leigh Syndrome 70 22.398
2
LBR002 Leber Hereditary Optic Neuropathy 59 21.117
3
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 27 18.288
4
P LCT001 Lactic Acidosis 52 16.695
5
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 16 16.695
6
P SDR003 Sideroblastic Anemia 40 16.695
7
P ATX004 Ataxia 53 16.695
8
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 10 16.695
9
c MYP107 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 10 16.695
10
KRN002 Kearns-Sayre Syndrome 60 14.932
11
P RTN008 Retinitis Pigmentosa 78 14.932
12
P NRP001 Neuropathy 57 14.932
13
P MYP108 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 17 14.932
14
P MTC069 Mitochondrial Disorders 51 12.932
15
CYS008 Cystic Echinococcosis 48 12.932
16
ECH003 Echinococcosis 53 12.932
17
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 12.932
18
MTC021 Mitochondrial Complex V Deficiency 16 12.932
19
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 10.559
20
LFT009 Left Ventricular Outflow Tract Obstruction 43 10.559
21
MTC005 Mitochondrial Metabolism Disease 37 10.559
22
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 27 10.559
23
P FML050 Familial Bilateral Striatal Necrosis 6 10.559
24
BYL001 Baylisascariasis 28 10.559
25
MLT132 Multifocal Dystonia 20 10.559
26
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 7.466
27
c FML309 Familial Infantile Bilateral Striatal Necrosis 13 7.466
28
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 15 7.466
29
MTR059 Maternally-Inherited Spastic Paraplegia 5 7.466