Search results for Phytanoyl-CoA

44 hits were found for Phytanoyl-CoA

# Family MCID Name MIFTS Score
1
RFS006 Refsum Disease, Classic 63 15.366
2
P RTN008 Retinitis Pigmentosa 80 6.665
3
NRR001 Neuroretinitis 42 6.665
4
RTN023 Retinitis 46 6.665
5
P CHN044 Chondrodysplasia Punctata Syndrome 43 6.607
6
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 6.607
7
SNS003 Sensory Peripheral Neuropathy 52 5.383
8
P ZLL001 Zellweger Syndrome 65 4.854
9
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.690
10
c BRN108 Branchiootic Syndrome 1 62 3.194
11
P PLY019 Polyneuropathy 52 3.194
12
P NRP001 Neuropathy 60 2.923
13
P PRP019 Peripheral Nervous System Disease 58 2.923
14
DWN001 Down Syndrome 70 2.603
15
PRX001 Peroxisomal Disease 46 2.258
16
c PRX045 Peroxisome Biogenesis Disorder 1b 62 2.184
17
FCT001 Factor Viii Deficiency 60 2.184
18
c HMP029 Hemophilia a 68 2.184
19
GLL048 Glial Tumor 52 2.184
20
GLB002 Glioblastoma 67 2.184
21
P HMP007 Hemophilia 52 2.184
22
GLM045 Glioma 63 2.184
23
P ICH004 Ichthyosis 56 2.019
24
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 45 1.749
25
ADR022 Adrenomyeloneuropathy 39 1.428
26
ADR007 Adrenoleukodystrophy 73 1.428
27
CRD223 Cardiac Arrhythmia 63 1.428
28
ATS010 Autosomal Recessive Disease 42 1.428
29
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.428
30
c PRX050 Peroxisome Biogenesis Disorder 9b 31 1.428
31
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.010
32
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.010
33
c RHZ014 Rhizomelic Chondrodysplasia Punctata, Type 2 44 1.010
34
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 53 1.010
35
P NRB001 Neuroblastoma 66 1.010
36
FTT001 Fatty Liver Disease 62 1.010
37
P MVM001 Movement Disease 61 1.010
38
P LVR013 Liver Disease 69 1.010
39
P RTN016 Retinal Degeneration 52 1.010
40
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.010
41
c INH020 Inherited Metabolic Disorder 48 1.010
42
NNT017 Neonatal Adrenoleukodystrophy 54 1.010
43
CNG065 Congenital Contractures 25 1.010
44
RFS003 Refsum Disease, Infantile Form 27 1.010
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