49 hits were found for 'MT-ND4'

# ++ Fam MCID Name MIFTS Score
1
P MLS001 Melas Syndrome 50 4.469
2
P LBR002 Leber Hereditary Optic Neuropathy 59 4.207
3
P MTC069 Mitochondrial Disorders 46 3.871
4
c LBR020 Leber Hereditary Optic Neuropathy with Dystonia 15 3.194
5
OPT009 Optic Neuritis 46 3.160
6
NRT004 Neuritis 46 3.160
7
LCT001 Lactic Acidosis 44 3.160
8
HRD088 Hereditary Neuropathies 35 3.160
9
P PRK002 Parkinson's Disease 86 2.737
10
c BLN003 Blindness 54 2.737
11
NRP001 Neuropathy 54 2.737
12
RTN023 Retinitis 53 2.737
13
c MYP004 Myopathy 52 2.737
14
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 2.737
15
CYS001 Cystic Fibrosis 91 2.280
16
P ALZ001 Alzheimer's Disease 93 2.235
17
ACT019 Acute Myeloid Leukemia 87 2.235
18
P RTN008 Retinitis Pigmentosa 76 2.235
19
P MLT020 Multiple Sclerosis 75 2.235
20
LKM002 Leukemia 70 2.235
21
c DBT009 Diabetes Mellitus 68 2.235
22
P CLR023 Colorectal Cancer 66 2.235
23
MYL006 Myeloid Leukemia 64 2.235
24
TRN018 Transitional Cell Carcinoma 61 2.235
25
P NRB001 Neuroblastoma 60 2.235
26
P ADN016 Adenocarcinoma 60 2.235
27
CHG001 Chagas Disease 58 2.235
28
P LGH001 Leigh Disease 56 2.235
29
ACN011 Acne 54 2.235
30
RNL014 Renal Cell Carcinoma 51 2.235
31
P OPN001 Open-Angle Glaucoma 51 2.235
32
P GLC007 Glaucoma 49 2.235
33
CRT012 Cortical Blindness 44 2.235
34
SPS057 Spasticity 42 2.235
35
ENC011 Encephalomyopathy 41 2.235
36
c OPT004 Optic Atrophy 41 2.235
37
CLN015 Colon Adenocarcinoma 41 2.235
38
MTC004 Mitochondrial Encephalomyopathy 38 2.235
39
CRR001 Carrion's Disease 32 2.235
40
c FML034 Familial Dystonia 25 2.235
41
TBR010 Tuberculosis 82 1.580
42
P MLT019 Multiple Myeloma 76 1.580
43
HPT023 Hepatocellular Carcinoma 69 1.580
44
P MLR004 Malaria 66 1.580
45
HYP266 Hypoxia 60 1.580
46
c MYL007 Myeloma 53 1.580
47
CRB009 Cerebritis 46 1.580
48
c PRP076 Porphyria Cutanea Tarda, Type Ii 17 1.580
49
DFN122 Deafness, Mitochondrial, Modifier of 15 1.580