Search results for "[genes] MT-ND4"

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

# Family MCID Name MIFTS Score
1
P NRP001 Neuropathy 60 18.049
2
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 18.049
3
LBR030 Leber Optic Atrophy 52 18.049
4
P LCT001 Lactic Acidosis 52 18.049
5
P LGH007 Leigh Syndrome 70 16.477
6
LBR020 Leber Hereditary Optic Neuropathy with Dystonia 30 16.477
7
P MTC004 Mitochondrial Encephalomyopathy 40 14.737
8
KRN002 Kearns-Sayre Syndrome 59 12.763
9
NRT004 Neuritis 52 12.763
10
OPT006 Optic Nerve Disease 51 12.763
11
OPT009 Optic Neuritis 48 12.763
12
P RTN008 Retinitis Pigmentosa 79 10.421
13
c OPT055 Optic Atrophy Plus Syndrome 54 10.421
14
P MTC069 Mitochondrial Disorders 52 10.421
15
AMB002 Amblyopia 46 10.421
16
P PRR025 Perrault Syndrome 41 10.421
17
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 40 10.421
18
CRN031 Cranial Nerve Disease 40 10.421
19
SCT002 Scotoma 39 10.421
20
MTC005 Mitochondrial Metabolism Disease 38 10.421
21
CRC001 Cercarial Dermatitis 37 10.421
22
CRR001 Carrion's Disease 37 10.421
23
CLR064 Colorblindness, Tritan 35 10.421
24
EXP002 Exposure Keratitis 27 10.421
25
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 27 10.421
26
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.421
27
CLN014 Colon Neuroendocrine Neoplasm 19 10.421
28
NTR002 Nutritional Optic Neuropathy 14 10.421
29
PRT024 Partial Optic Atrophy 13 10.421
30
P NRV007 Nervous System Disease 71 7.369
31
MTC007 Mitochondrial Complex I Deficiency 61 7.369
32
DFN122 Deafness, Mitochondrial, Modifier of 26 7.369