Search results for "[genes] MT-ND4"

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

# Family MCID Name MIFTS Score
1
LBR002 Leber Hereditary Optic Neuropathy 59 21.936
2
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 17.911
3
P NRP001 Neuropathy 57 17.911
4
P LGH007 Leigh Syndrome 70 16.350
5
LBR020 Leber Hereditary Optic Neuropathy with Dystonia 31 16.350
6
P LCT001 Lactic Acidosis 52 16.350
7
P MTC004 Mitochondrial Encephalomyopathy 39 14.624
8
KRN002 Kearns-Sayre Syndrome 60 12.665
9
OPT009 Optic Neuritis 48 12.665
10
NRT004 Neuritis 52 12.665
11
c OPT055 Optic Atrophy Plus Syndrome 55 10.341
12
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 42 10.341
13
c CHR095 Chronic Progressive External Ophthalmoplegia 48 10.341
14
P PRR025 Perrault Syndrome 42 10.341
15
ERL001 Early Myoclonic Encephalopathy 46 10.341
16
P MTC069 Mitochondrial Disorders 51 10.341
17
OPT006 Optic Nerve Disease 47 10.341
18
CRC001 Cercarial Dermatitis 40 10.341
19
CRR001 Carrion's Disease 37 10.341
20
SCT002 Scotoma 37 10.341
21
AMB002 Amblyopia 42 10.341
22
CRN031 Cranial Nerve Disease 39 10.341
23
CRT012 Cortical Blindness 36 10.341
24
BLC005 Blue Color Blindness 27 10.341
25
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 10.341
26
LWN001 Lown-Ganong-Levine Syndrome 28 10.341
27
EXP002 Exposure Keratitis 27 10.341
28
CLN014 Colon Neuroendocrine Neoplasm 18 10.341
29
NTR002 Nutritional Optic Neuropathy 14 10.341
30
PRT024 Partial Optic Atrophy 12 10.341
31
NNT041 Neonatal Period Electroclinical Syndrome 19 10.341
32
MTC007 Mitochondrial Complex I Deficiency 61 7.312
33
P NRV007 Nervous System Disease 71 7.312
34
DFN122 Deafness, Mitochondrial, Modifier of 27 7.312