Search results for "[genes] MT-ND4"

36 hits were found for '[genes] MT-ND4'

# Family MCID Name MIFTS Score
1
P LGH007 Leigh Syndrome 70 19.234
2
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 19.234
3
LBR030 Leber Optic Atrophy 53 19.234
4
P NRP001 Neuropathy 59 17.807
5
P LCT001 Lactic Acidosis 51 17.807
6
LBR020 Leber Hereditary Optic Neuropathy with Dystonia 29 16.256
7
KRN002 Kearns-Sayre Syndrome 61 14.540
8
NRT004 Neuritis 52 14.540
9
OPT006 Optic Nerve Disease 52 14.540
10
OPT009 Optic Neuritis 50 14.540
11
P MTC004 Mitochondrial Encephalomyopathy 42 14.540
12
P RTN008 Retinitis Pigmentosa 80 12.592
13
P MTC069 Mitochondrial Disorders 53 12.592
14
c OPT055 Optic Atrophy Plus Syndrome 52 12.592
15
AMB002 Amblyopia 46 12.592
16
SCT002 Scotoma 40 12.592
17
CRN031 Cranial Nerve Disease 40 12.592
18
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 39 12.592
19
P ENC011 Encephalomyopathy 37 12.592
20
MTC005 Mitochondrial Metabolism Disease 36 12.592
21
CRC001 Cercarial Dermatitis 35 12.592
22
CRR001 Carrion's Disease 34 12.592
23
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 27 12.592
24
EXP002 Exposure Keratitis 26 12.592
25
DFN122 Deafness, Mitochondrial, Modifier of 26 12.592
26
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 12.592
27
CLN014 Colon Neuroendocrine Neoplasm 17 12.592
28
NTR002 Nutritional Optic Neuropathy 14 12.592
29
PRT024 Partial Optic Atrophy 14 12.592
30
P NRV007 Nervous System Disease 71 10.281
31
MTC007 Mitochondrial Complex I Deficiency 61 10.281
32
c RTN142 Retinitis Pigmentosa 38 36 10.281
33
c 3MT014 3-Methylglutaconic Aciduria, Type V 36 10.281
34
CLR064 Colorblindness, Tritan 32 10.281
35
BLC005 Blue Color Blindness 29 10.281
36
PRP019 Peripheral Nervous System Disease 55 7.270