Search results for "[genes] MT-CO1"

47 hits were found for '[genes] MT-CO1'

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 91 17.225
2
LBR002 Leber Hereditary Optic Neuropathy 56 17.225
3
P LGH007 Leigh Syndrome 66 15.725
4
MTC097 Mitochondrial Complex Iv Deficiency 47 15.725
5
MCR264 Mcardle Disease 51 12.180
6
ALV002 Alveolar Echinococcosis 51 12.180
7
MGL001 Megaloblastic Anemia 49 12.180
8
ECH003 Echinococcosis 49 12.180
9
KRN002 Kearns-Sayre Syndrome 52 9.945
10
P MLS001 Melas Syndrome 50 9.945
11
P MTC069 Mitochondrial Disorders 48 9.945
12
CYS008 Cystic Echinococcosis 46 9.945
13
CRC001 Cercarial Dermatitis 43 9.945
14
MTR046 Maternally Inherited Diabetes and Deafness 42 9.945
15
PRS036 Parasitic Protozoa Infectious Disease 42 9.945
16
CYS005 Cysticercosis 40 9.945
17
DRF001 Dirofilariasis 39 9.945
18
FSC002 Fascioliasis 39 9.945
19
PRS034 Parasitic Helminthiasis Infectious Disease 38 9.945
20
PRG008 Paragonimiasis 37 9.945
21
SRC011 Sarcocystosis 35 9.945
22
SPR006 Sparganosis 35 9.945
23
LCN001 Lice Infestation 34 9.945
24
TNS007 Taeniasis 34 9.945
25
MYS004 Myiasis 34 9.945
26
DPH003 Diphyllobothriasis 34 9.945
27
HYM001 Hymenolepiasis 33 9.945
28
c CHR091 Chronic Meningitis 31 9.945
29
CNR001 Coenurosis 29 9.945
30
BYL001 Baylisascariasis 28 9.945
31
OPH001 Ophthalmomyiasis 26 9.945
32
PTH001 Pthirus Pubis Infestation 25 9.945
33
GNT004 Gnathomiasis 24 9.945
34
ACQ031 Acquired Idiopathic Sideroblastic Anemia 23 9.945
35
FTL003 Fatal Infantile Encephalocardiomyopathy 22 9.945
36
NNS014 Nonsyndromic Hearing Loss and Deafness 20 9.945
37
DFN003 Deafness and Hereditary Hearing Loss 19 9.945
38
PDC002 Pediculus Humanus Capitis Infestation 19 9.945
39
PRS033 Parasitic Ectoparasitic Infectious Disease 15 9.945
40
NNS010 Nonsyndromic Hearing Loss and Deafness, Mitochondrial 12 9.945
41
MSC001 Mesocestoidiasis 7 9.945
42
ISL083 Isolated Cytochrome C Oxidase Deficiency 29 7.032
43
c MYG003 Myoglobinuria Recurrent 18 7.032
44
MTC101 Mitochondrial Non-Syndromic Sensorineural Deafness with Susceptibility to Aminoglycoside Exposure 15 7.032
45
MTC106 Mitochondrial Non-Syndromic Sensorineural Deafness 14 7.032
46
GNT042 Genetic Recurrent Myoglobinuria 13 7.032
47
MTC052 Mt-Co1-Related Hearing Loss and Deafness 3 7.032