Search results for "[genes] MT-CO1"

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

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 97 17.070
2
MTC097 Mitochondrial Complex Iv Deficiency 51 17.070
3
LBR030 Leber Optic Atrophy 53 15.583
4
P LGH007 Leigh Syndrome 70 13.937
5
MCR264 Mcardle Disease 56 13.937
6
ECH003 Echinococcosis 54 13.937
7
ALV002 Alveolar Echinococcosis 46 13.937
8
CYS008 Cystic Echinococcosis 46 13.937
9
P SDR003 Sideroblastic Anemia 40 13.937
10
P MYG005 Myoglobinuria 35 13.937
11
MLR004 Malaria 83 12.070
12
CYS005 Cysticercosis 54 12.070
13
P MTC069 Mitochondrial Disorders 53 12.070
14
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 12.070
15
TNS007 Taeniasis 41 12.070
16
PRS036 Parasitic Protozoa Infectious Disease 41 12.070
17
PRG008 Paragonimiasis 40 12.070
18
PRS034 Parasitic Helminthiasis Infectious Disease 38 12.070
19
DRF001 Dirofilariasis 37 12.070
20
CRC001 Cercarial Dermatitis 35 12.070
21
SPR006 Sparganosis 34 12.070
22
MYS004 Myiasis 33 12.070
23
HYM001 Hymenolepiasis 31 12.070
24
LCN001 Lice Infestation 31 12.070
25
NNS014 Nonsyndromic Hearing Loss and Deafness 28 12.070
26
DPH003 Diphyllobothriasis 28 12.070
27
DFN122 Deafness, Mitochondrial, Modifier of 26 12.070
28
CNR001 Coenurosis 25 12.070
29
PDC002 Pediculus Humanus Capitis Infestation 23 12.070
30
OPH001 Ophthalmomyiasis 23 12.070
31
FTL003 Fatal Infantile Encephalocardiomyopathy 23 12.070
32
c MYG003 Myoglobinuria Recurrent 23 12.070
33
ACQ031 Acquired Idiopathic Sideroblastic Anemia 21 12.070
34
GNT004 Gnathomiasis 20 12.070
35
PRS033 Parasitic Ectoparasitic Infectious Disease 19 12.070
36
PTH001 Pthirus Pubis Infestation 18 12.070
37
MTC106 Mitochondrial Non-Syndromic Sensorineural Deafness 15 12.070
38
GNT042 Genetic Recurrent Myoglobinuria 13 12.070
39
NNS010 Nonsyndromic Hearing Loss and Deafness, Mitochondrial 10 12.070
40
MSC001 Mesocestoidiasis 5 12.070
41
MTC052 Mt-Co1-Related Hearing Loss and Deafness 3 12.070
42
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 9.855
43
NRW001 Norwegian Scabies 42 9.855
44
c MYS052 Myasthenic Syndrome, Congenital, 10 40 9.855
45
c CRD190 Cardiomyopathy, Hypertrophic, 2 39 9.855
46
c AML020 Amelogenesis Imperfecta, Type Iv 33 9.855
47
c RTN083 Retinitis Pigmentosa-40 33 9.855
48
SRC011 Sarcocystosis 29 9.855
49
c HLP023 Holoprosencephaly 1 25 9.855