Search results for "[genes] MT-ND1"

39 hits were found for '[genes] MT-ND1'

# Family MCID Name MIFTS Score
1
LBR002 Leber Hereditary Optic Neuropathy 58 23.914
2
MTC007 Mitochondrial Complex I Deficiency 57 17.662
3
P MLS001 Melas Syndrome 53 17.662
4
P NRP001 Neuropathy 48 17.662
5
P LCT001 Lactic Acidosis 40 17.662
6
P ALZ034 Alzheimer Disease 98 16.123
7
P MTC004 Mitochondrial Encephalomyopathy 32 16.123
8
P LGH007 Leigh Syndrome 67 14.421
9
OPT006 Optic Nerve Disease 39 14.421
10
CRN031 Cranial Nerve Disease 30 14.421
11
ALZ029 Alzheimer Disease Mitochondrial 25 14.421
12
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 12.489
13
c PRK057 Parkinson Disease, Late-Onset 73 12.489
14
WST001 West Syndrome 54 12.489
15
P CRD011 Cardiomyopathy 53 12.489
16
LNN001 Lennox-Gastaut Syndrome 44 12.489
17
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 10.197
18
P SDD001 Sudden Infant Death Syndrome 59 10.197
19
CYS008 Cystic Echinococcosis 51 10.197
20
P MTC069 Mitochondrial Disorders 49 10.197
21
ARC002 Arachnoiditis 43 10.197
22
TNC002 Tinea Capitis 42 10.197
23
ISC002 Ischemic Optic Neuropathy 38 10.197
24
PRS034 Parasitic Helminthiasis Infectious Disease 36 10.197
25
MYS004 Myiasis 35 10.197
26
PHL003 Phlebotomus Fever 35 10.197
27
CRT012 Cortical Blindness 32 10.197
28
TNS007 Taeniasis 30 10.197
29
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 10.197
30
CNR001 Coenurosis 27 10.197
31
c FTL032 Fatal Infantile Lactic Acidosis 17 10.197
32
c ALZ037 Alzheimer Disease-2 52 7.210
33
LBR020 Leber Hereditary Optic Neuropathy with Dystonia 30 7.210
34
MTR017 Maternally Inherited Leigh Syndrome 30 7.210
35
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 27 7.210
36
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 7.210
37
LBR030 Leber Optic Atrophy 24 7.210
38
MTC106 Mitochondrial Non-Syndromic Sensorineural Deafness 18 7.210
39
c MLS003 Melas, Mt-Nd1-Related 7 7.210