Search results for "[genes] MT-ATP6"

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

# Family MCID Name MIFTS Score
1
P LGH007 Leigh Syndrome 70 21.976
2
P MTC069 Mitochondrial Disorders 53 19.381
3
LBR030 Leber Optic Atrophy 53 17.943
4
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 27 17.943
5
P RTN008 Retinitis Pigmentosa 80 16.380
6
KRN002 Kearns-Sayre Syndrome 61 16.380
7
P ATX004 Ataxia 53 16.380
8
P LCT001 Lactic Acidosis 51 16.380
9
P SDR003 Sideroblastic Anemia 40 16.380
10
MTC080 Mitochondrial Complex V Deficiency, Mitochondrial 1 16 16.380
11
c MYP107 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 10 16.380
12
MTC081 Mitochondrial Infantile Bilateral Striatal Necrosis 10 16.380
13
P CHR071 Charcot-Marie-Tooth Disease 67 14.651
14
P NRP001 Neuropathy 59 14.651
15
ECH003 Echinococcosis 54 14.651
16
CYS008 Cystic Echinococcosis 46 14.651
17
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 14.651
18
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 14.651
19
P MYP108 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 16 14.651
20
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 12.688
21
RSS002 Roussy-Levy Syndrome 50 12.688
22
MTC005 Mitochondrial Metabolism Disease 36 12.688
23
BYL001 Baylisascariasis 27 12.688
24
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 20 12.688
25
MTC021 Mitochondrial Complex V Deficiency 16 12.688
26
c FML309 Familial Infantile Bilateral Striatal Necrosis 13 12.688
27
PRD033 Periodic Paralysis with Later-Onset Distal Motor Neuropathy 13 12.688
28
MTR059 Maternally-Inherited Spastic Paraplegia 6 12.688
29
P FML050 Familial Bilateral Striatal Necrosis 6 12.688
30
LFT009 Left Ventricular Outflow Tract Obstruction 43 10.360
31
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 10.360
32
MNT192 Mental Retardation, X-Linked, Syndromic, Hedera Type 30 10.360
33
c BRT038 Baraitser-Winter Syndrome 1 35 7.325
34
CMP039 Camptodactyly 1 16 7.325