49 hits were found for 'MT-ND4'

# Family MCID Name MIFTS Score
1
P MLS001 Melas Syndrome 61 4.466
2
LBR002 Leber Hereditary Optic Neuropathy 63 4.203
3
MTC069 Mitochondrial Disorders 47 3.867
4
LBR020 Leber Hereditary Optic Neuropathy with Dystonia 21 3.192
5
OPT009 Optic Neuritis 53 3.158
6
NRT004 Neuritis 51 3.158
7
LCT001 Lactic Acidosis 49 3.158
8
HRD088 Hereditary Neuropathies 31 3.158
9
P PRK002 Parkinson's Disease 92 2.735
10
RTN023 Retinitis 61 2.735
11
NRP001 Neuropathy 61 2.735
12
P MYP004 Myopathy 58 2.735
13
c BLN003 Blindness 37 2.735
14
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 28 2.735
15
CYS001 Cystic Fibrosis 103 2.278
16
P ALZ001 Alzheimer's Disease 103 2.233
17
P ACT019 Acute Myeloid Leukemia 94 2.233
18
P MLT020 Multiple Sclerosis 82 2.233
19
P RTN008 Retinitis Pigmentosa 81 2.233
20
c DBT009 Diabetes Mellitus 80 2.233
21
P LKM002 Leukemia 79 2.233
22
P CLR023 Colorectal Cancer 73 2.233
23
c MYL006 Myeloid Leukemia 72 2.233
24
P NRB001 Neuroblastoma 71 2.233
25
P LGH001 Leigh Disease 67 2.233
26
CHG001 Chagas Disease 66 2.233
27
TRN018 Transitional Cell Carcinoma 64 2.233
28
P ADN016 Adenocarcinoma 60 2.233
29
P RNL014 Renal Cell Carcinoma 59 2.233
30
P GLC007 Glaucoma 58 2.233
31
c OPN001 Open-Angle Glaucoma 56 2.233
32
ACN011 Acne 56 2.233
33
CLN015 Colon Adenocarcinoma 48 2.233
34
c OPT004 Optic Atrophy 46 2.233
35
CRT012 Cortical Blindness 45 2.233
36
MTC004 Mitochondrial Encephalomyopathy 43 2.233
37
CRR001 Carrion's Disease 37 2.233
38
c FML034 Familial Dystonia 32 2.233
39
ENC011 Encephalomyopathy 29 2.233
40
SPS057 Spasticity 29 2.233
41
P MLT019 Multiple Myeloma 89 1.579
42
HPT023 Hepatocellular Carcinoma 89 1.579
43
TBR010 Tuberculosis 84 1.579
44
P MLR004 Malaria 73 1.579
45
c MYL007 Myeloma 59 1.579
46
CRB009 Cerebritis 56 1.579
47
HYP266 Hypoxia 43 1.579
48
c PRP076 Porphyria Cutanea Tarda, Type Ii 27 1.579
49
DFN122 Deafness, Mitochondrial, Modifier of 23 1.579