Search results for (2E)-Hexadecenoyl-CoA

81 hits were found for (2E)-Hexadecenoyl-CoA

# Family MCID Name MIFTS Score
1
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 9.359
2
c MSC114 Muscular Dystrophy, Limb-Girdle, Type 2e 43 6.960
3
WRD025 Waardenburg Syndrome, Type 2e, with or Without Neurologic Involvement 42 6.585
4
c PNT034 Pontocerebellar Hypoplasia, Type 2e 34 6.169
5
c CNG412 Congenital Disorder of Glycosylation, Type Ii 46 4.631
6
c PSD092 Pseudohypoaldosteronism, Type Iie 38 4.631
7
c CHR520 Charcot-Marie-Tooth Disease, Axonal, Type 2s 36 2.351
8
P ICH004 Ichthyosis 52 0.221
9
ICH002 Ichthyosis Bullosa of Siemens 45 0.221
10
P CHR071 Charcot-Marie-Tooth Disease 67 0.187
11
TTH006 Tooth Disease 52 0.187
12
P MSC005 Muscular Dystrophy 65 0.177
13
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.177
14
HPT074 Hepatic Adenoma, Somatic 50 0.118
15
ADP007 Adie Pupil 34 0.118
16
HNM002 Hinman Syndrome 25 0.118
17
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.102
18
AND005 Androgen Insensitivity Syndrome, Mild 16 0.102
19
P DYS154 Dystonia 65 0.084
20
P NRP001 Neuropathy 59 0.084
21
P ATX004 Ataxia 53 0.084
22
RTN023 Retinitis 50 0.084
23
CHR073 Choreatic Disease 37 0.084
24
SRC016 Sarcoglycanopathies 33 0.084
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.084
26
P RTN008 Retinitis Pigmentosa 80 0.059
27
P NRV007 Nervous System Disease 71 0.059
28
WRN001 Werner Syndrome 67 0.059
29
P MYP004 Myopathy 67 0.059
30
P EPL164 Epilepsy 66 0.059
31
P KLL001 Kallmann Syndrome 61 0.059
32
P PSR002 Psoriasis 61 0.059
33
WLL001 Williams-Beuren Syndrome 60 0.059
34
P MCR010 Microcephaly 58 0.059
35
SNS001 Sensorineural Hearing Loss 57 0.059
36
CNG008 Congenital Ichthyosiform Erythroderma 56 0.059
37
P PLY019 Polyneuropathy 56 0.059
38
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.059
39
HYP080 Hypogonadism 53 0.059
40
RTN018 Retinal Disease 53 0.059
41
c WRD030 Waardenburg Syndrome, Type 1 51 0.059
42
KLN001 Klinefelter's Syndrome 50 0.059
43
P INT063 Intellectual Disability 49 0.059
44
DYS073 Dysphagia 48 0.059
45
ALB002 Albinism 46 0.059
46
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 44 0.059
47
P DMY001 Demyelinating Polyneuropathy 43 0.059
48
P CRB088 Cerebral Atrophy 42 0.059
49
SPS057 Spasticity 42 0.059
50
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.059
51
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.059
52
c RTN150 Retinitis Pigmentosa 10 41 0.059
53
PRX075 Proximal Myopathy and Ophthalmoplegia 41 0.059
54
NRN002 Neuronitis 41 0.059
55
c RTN043 Retinitis Pigmentosa 13 40 0.059
56
CRB009 Cerebritis 39 0.059
57
NRP016 Neuropathy, Recurrent, with Pressure Palsies 38 0.059
58
P PNT019 Pontocerebellar Hypoplasia 38 0.059
59
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.059
60
P AXN001 Axonal Neuropathy 38 0.059
61
MTR007 Motor Peripheral Neuropathy 37 0.059
62
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 37 0.059
63
CLD014 Cole Disease 37 0.059
64
HYP064 Hypogonadotropism 37 0.059
65
TTR016 Tetra-Amelia Syndrome 36 0.059
66
CLP001 Calpainopathy 36 0.059
67
ALR002 Al-Raqad Syndrome 36 0.059
68
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.059
69
c RTN070 Retinitis Pigmentosa 9 35 0.059
70
c WRD032 Waardenburg Syndrome, Type 2a 34 0.059
71
c RTN047 Retinitis Pigmentosa 18 34 0.059
72
c BRN108 Branchiootic Syndrome 1 34 0.059
73
c RTN041 Retinitis Pigmentosa 11 33 0.059
74
CHR423 Chorea, Hereditary Benign 31 0.059
75
c PNT029 Pontocerebellar Hypoplasia Type 2d 31 0.059
76
c PNT022 Pontocerebellar Hypoplasia Type 2a 30 0.059
77
c WRD031 Waardenburg Syndrome, Type 3 29 0.059
78
HYP213 Hypomelanotic Disorder 21 0.059
79
c RTN161 Retinitis Pigmentosa, X-Linked Recessive, 6 21 0.059
80
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 21 0.059
81
HTR005 Heterochromia Iridis 18 0.059
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