Search results for NDUFA1

22 hits were found for NDUFA1

# Family MCID Name MIFTS Score
1
MTC147 Mitochondrial Complex I Deficiency, Nuclear Type 12 20 5.447
2
LGH007 Leigh Syndrome 70 4.350
3
P MTC004 Mitochondrial Encephalomyopathy 44 3.704
4
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 3.199
5
P OPT006 Optic Nerve Disease 60 3.008
6
MTC005 Mitochondrial Metabolism Disease 49 3.008
7
P MYP004 Myopathy 70 2.952
8
LBR030 Leber Optic Atrophy 60 2.952
9
P LKD001 Leukodystrophy 59 2.952
10
P MTC069 Mitochondrial Disorders 56 2.160
11
c FNC027 Fanconi Anemia, Complementation Group a 81 2.088
12
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 2.088
13
P MTC133 Mitochondrial Myopathy 49 2.088
14
CRD231 Cardiomyopathy, Infantile Histiocytoid 45 2.088
15
EXP002 Exposure Keratitis 26 2.088
16
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.124
17
c BSL007 Basal Cell Carcinoma 68 0.087
18
P CRN300 Coronary Heart Disease 1 63 0.087
19
ERL001 Early Myoclonic Encephalopathy 62 0.087
20
P LCT001 Lactic Acidosis 51 0.087
21
P HYP265 Hypotonia 43 0.087
22
NCL007 Nuclear Gene-Encoded Leigh Syndrome 22 0.087
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