Search results for mt-co1

Showing 25 of 221 hits for mt-co1
# Family MCID Name MIFTS Score
26
P HYP061 Hypertrophic Cardiomyopathy 69 8.128
27
KRT058 Keratoderma, Palmoplantar, with Deafness 44 7.529
28
LBR036 Leber Plus Disease 70 7.529
29
ISL083 Isolated Cytochrome C Oxidase Deficiency 28 7.529
30
GNT042 Genetic Recurrent Myoglobinuria 24 7.529
31
P OPT006 Optic Nerve Disease 56 7.238
32
CYS008 Cystic Echinococcosis 53 6.846
33
ALV002 Alveolar Echinococcosis 54 6.810
34
P LCT001 Lactic Acidosis 51 6.026
35
MTC004 Mitochondrial Encephalomyopathy 42 6.026
36
ANG002 Angiostrongyliasis 43 5.945
37
c CHR095 Chronic Progressive External Ophthalmoplegia 49 5.945
38
MYS004 Myiasis 40 5.945
39
c HLP023 Holoprosencephaly 1 56 5.747
40
c NML004 Nemaline Myopathy 3 47 5.747
41
OSB001 Osebold-Remondini Syndrome 35 5.747
42
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 5.747
43
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 48 5.747
44
DFN350 Deafness, Aminoglycoside-Induced 33 5.747
45
c MYP107 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 23 5.747
46
c PSR032 Psoriasis 11 57 5.747
47
END014 Endemic Typhus 32 5.747
48
STT041 Stuttering 53 5.747
49
c ATM006 Autoimmune Lymphoproliferative Syndrome 72 5.747
50
c EPL115 Epilepsy, Familial Temporal Lobe, 2 40 5.747
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