Search results for "[genes] MT-ND1"

35 hits were found for '[genes] MT-ND1'

# Family MCID Name MIFTS Score
1
LBR002 Leber Hereditary Optic Neuropathy 59 21.851
2
MTC007 Mitochondrial Complex I Deficiency 61 17.842
3
P LCT001 Lactic Acidosis 52 16.287
4
P ALZ034 Alzheimer Disease 92 14.568
5
P LGH007 Leigh Syndrome 70 14.568
6
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 14.568
7
P MTC004 Mitochondrial Encephalomyopathy 39 14.568
8
P NRP001 Neuropathy 57 14.568
9
ALZ029 Alzheimer Disease Mitochondrial 25 14.568
10
P PRK057 Parkinson Disease, Late-Onset 72 12.616
11
WST001 West Syndrome 61 12.616
12
P SDD001 Sudden Infant Death Syndrome 60 12.616
13
LNN001 Lennox-Gastaut Syndrome 51 12.616
14
DXT001 Dextrocardia 44 12.616
15
P MTC069 Mitochondrial Disorders 51 10.301
16
CYS005 Cysticercosis 52 10.301
17
PRS034 Parasitic Helminthiasis Infectious Disease 47 10.301
18
P LFT003 Left Ventricular Noncompaction 48 10.301
19
OPT006 Optic Nerve Disease 47 10.301
20
CYS008 Cystic Echinococcosis 48 10.301
21
ECH003 Echinococcosis 53 10.301
22
P CRD011 Cardiomyopathy 66 10.301
23
PHL003 Phlebotomus Fever 31 10.301
24
ARC002 Arachnoiditis 38 10.301
25
TNS007 Taeniasis 41 10.301
26
CRN031 Cranial Nerve Disease 39 10.301
27
TRC062 Tricuspid Atresia 34 10.301
28
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.301
29
CNR001 Coenurosis 24 10.301
30
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 10.301
31
ISC002 Ischemic Optic Neuropathy 45 10.301
32
c FTL032 Fatal Infantile Lactic Acidosis 15 10.301
33
LBR020 Leber Hereditary Optic Neuropathy with Dystonia 31 7.284
34
LBR030 Leber Optic Atrophy 22 7.284
35
c MLS003 Melas, Mt-Nd1-Related 3 7.284