Search results for "[genes] MT-ATP6"

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

# Family MCID Name MIFTS Score
1
P LGH007 Leigh Syndrome 70 22.016
2
P MTC069 Mitochondrial Disorders 52 17.976
3
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 27 17.976
4
P RTN008 Retinitis Pigmentosa 79 16.410
5
P ATX004 Ataxia 53 16.410
6
LBR030 Leber Optic Atrophy 52 16.410
7
P LCT001 Lactic Acidosis 52 16.410
8
P SDR003 Sideroblastic Anemia 39 16.410
9
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 16 16.410
10
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 11 16.410
11
c MYP107 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 10 16.410
12
P NRP001 Neuropathy 60 14.677
13
KRN002 Kearns-Sayre Syndrome 59 14.677
14
P MYP108 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 16 14.677
15
P CHR071 Charcot-Marie-Tooth Disease 66 12.711
16
ECH003 Echinococcosis 53 12.711
17
CYS008 Cystic Echinococcosis 50 12.711
18
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 12.711
19
MTC021 Mitochondrial Complex V Deficiency 16 12.711
20
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 10.378
21
LFT009 Left Ventricular Outflow Tract Obstruction 44 10.378
22
MTC005 Mitochondrial Metabolism Disease 38 10.378
23
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 37 10.378
24
BYL001 Baylisascariasis 27 10.378
25
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 23 10.378
26
P FML050 Familial Bilateral Striatal Necrosis 5 10.378
27
RSS002 Roussy-Levy Syndrome 52 7.339
28
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 51 7.339
29
P CHR102 Charcot-Marie-Tooth Neuropathy 43 7.339
30
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 7.339
31
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 14 7.339
32
c FML309 Familial Infantile Bilateral Striatal Necrosis 12 7.339
33
MTR059 Maternally-Inherited Spastic Paraplegia 6 7.339