Search results for "[genes] MT-ATP6"

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

# Family MCID Name MIFTS Score
1
P LGH007 Leigh Syndrome 66 21.518
2
LBR002 Leber Hereditary Optic Neuropathy 56 21.518
3
P MTC069 Mitochondrial Disorders 48 18.635
4
P RTN008 Retinitis Pigmentosa 75 17.011
5
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 11 17.011
6
c MYP107 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 11 17.011
7
P NRP001 Neuropathy 47 15.215
8
P LCT001 Lactic Acidosis 41 15.215
9
P SDR003 Sideroblastic Anemia 37 15.215
10
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 17 15.215
11
P CRD011 Cardiomyopathy 59 13.177
12
KRN002 Kearns-Sayre Syndrome 52 13.177
13
ECH003 Echinococcosis 49 13.177
14
CYS008 Cystic Echinococcosis 46 13.177
15
NRP003 Neuropathy Ataxia Retinitis Pigmentosa Syndrome 28 13.177
16
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 27 13.177
17
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 26 13.177
18
P MYP108 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 16 13.177
19
MTC021 Mitochondrial Complex V Deficiency 15 13.177
20
P MLS001 Melas Syndrome 50 10.759
21
HMP005 Hemiplegia 42 10.759
22
LFT009 Left Ventricular Outflow Tract Obstruction 42 10.759
23
MTC005 Mitochondrial Metabolism Disease 29 10.759
24
c FML309 Familial Infantile Bilateral Striatal Necrosis 15 7.608
25
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 14 7.608
26
MTR059 Maternally-Inherited Spastic Paraplegia 5 7.608