Search results for (2E)-Hexadecenoyl-CoA

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

# Family MCID Name MIFTS Score
1
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 54 10.076
2
c WRD033 Waardenburg Syndrome, Type 2e 51 7.262
3
c MSC121 Muscular Dystrophy, Limb-Girdle, Type 2a 58 6.673
4
c PNT034 Pontocerebellar Hypoplasia, Type 2e 40 5.813
5
c PSD092 Pseudohypoaldosteronism, Type Iie 36 4.882
6
c ATS359 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e 37 4.514
7
c CNG412 Congenital Disorder of Glycosylation, Type Ii 46 3.791
8
c ART054 Arthrogryposis, Distal, Type 2e 16 2.239
9
GNY003 Guanylate Cyclase 2e, Pseudogene 7 2.239
10
P ICH004 Ichthyosis 54 0.164
11
ICH002 Ichthyosis Bullosa of Siemens 48 0.164
12
P MSC005 Muscular Dystrophy 66 0.158
13
P LMB006 Limb-Girdle Muscular Dystrophy 54 0.158
14
P CHR071 Charcot-Marie-Tooth Disease 65 0.145
15
TTH006 Tooth Disease 53 0.145
16
P ANR048 Aniridia 1 65 0.088
17
HPT082 Hepatic Adenomas, Familial 53 0.088
18
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.088
19
BLD137 Blood Group--Ahonen 17 0.088
20
NRM005 Neuromuscular Disease 60 0.076
21
ADP007 Adie Pupil 41 0.076
22
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.076
23
P MYP004 Myopathy 68 0.062
24
P NRP001 Neuropathy 63 0.062
25
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 58 0.062
26
P MSC033 Muscle Disorders 52 0.062
27
MSC004 Muscle Tissue Disease 39 0.062
28
ALR002 Al-Raqad Syndrome 31 0.062
29
c BLD140 Blood Group, I System 23 0.062
30
ATR076 Atrophic Muscular Disease 18 0.062
31
P RTN008 Retinitis Pigmentosa 81 0.044
32
ALP046 Alport Syndrome, X-Linked 75 0.044
33
P NRV007 Nervous System Disease 73 0.044
34
CRB037 Cerebral Palsy 71 0.044
35
WRN001 Werner Syndrome 69 0.044
36
P EPL164 Epilepsy 69 0.044
37
EWN003 Ewing Sarcoma 68 0.044
38
c HRD010 Hereditary Spastic Paraplegia 67 0.044
39
P PSR002 Psoriasis 65 0.044
40
NRF007 Neurofibroma 65 0.044
41
P DYS154 Dystonia 64 0.044
42
AGN016 Aging 64 0.044
43
WLL001 Williams-Beuren Syndrome 63 0.044
44
MST017 Mast Cell Disease 63 0.044
45
P KLL001 Kallmann Syndrome 63 0.044
46
P HRS035 Hirschsprung Disease 1 62 0.044
47
MTR014 Motor Neuron Disease 61 0.044
48
MCR013 Microphthalmia 60 0.044
49
CNG008 Congenital Ichthyosiform Erythroderma 60 0.044
50
VNW001 Von Willebrand's Disease 60 0.044
51
PRP019 Peripheral Nervous System Disease 60 0.044
52
P WRD001 Waardenburg's Syndrome 58 0.044
53
P PLY019 Polyneuropathy 57 0.044
54
c INT072 Intestinal Pseudo-Obstruction 57 0.044
55
P MCR010 Microcephaly 57 0.044
56
SNS001 Sensorineural Hearing Loss 56 0.044
57
HYP730 Hypogonadotropic Hypogonadism 56 0.044
58
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.044
59
P MSC003 Muscular Atrophy 54 0.044
60
PBL005 Piebald Trait 54 0.044
61
CLN019 Colonic Disease 54 0.044
62
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.044
63
PRP016 Paraplegia 53 0.044
64
SNS003 Sensory Peripheral Neuropathy 53 0.044
65
P CNT004 Centronuclear Myopathy 53 0.044
66
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 52 0.044
67
P HRD018 Hair Disease 51 0.044
68
HYP080 Hypogonadism 51 0.044
69
c MSC120 Muscular Dystrophy, Limb-Girdle, Type 2c 51 0.044
70
c WRD030 Waardenburg Syndrome, Type 1 51 0.044
71
RTN023 Retinitis 50 0.044
72
NRP060 Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive 50 0.044
73
MGC001 Megacolon 49 0.044
74
c LBR014 Leber Congenital Amaurosis 4 49 0.044
75
DYS022 Dyschromatosis Symmetrica Hereditaria 49 0.044
76
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 48 0.044
77
c DWL002 Dowling-Degos Disease 1 48 0.044
78
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 47 0.044
79
P OCL001 Ocular Albinism 46 0.044
80
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.044
81
P DMY001 Demyelinating Polyneuropathy 46 0.044
82
DYS073 Dysphagia 46 0.044
83
ALB002 Albinism 46 0.044
84
c WRD020 Waardenburg Syndrome, Type 4a 45 0.044
85
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 45 0.044
86
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 45 0.044
87
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.044
88
TTZ003 Tietz Albinism-Deafness Syndrome 44 0.044
89
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 44 0.044
90
c CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 44 0.044
91
MYP136 Myopathy, Centronuclear, X-Linked 44 0.044
92
c MSC123 Muscular Dystrophy, Limb-Girdle, Type 2d 44 0.044
93
c MSC116 Muscular Dystrophy, Limb-Girdle, Type 2f 43 0.044
94
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 43 0.044
95
CHR629 Charcot-Marie-Tooth Disease and Deafness 42 0.044
96
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 42 0.044
97
MYC033 Myoclonus 41 0.044
98
P PNT019 Pontocerebellar Hypoplasia 41 0.044
99
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 41 0.044
100
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 41 0.044
101
NRN002 Neuronitis 41 0.044
102
CRB009 Cerebritis 41 0.044
103
SPS057 Spasticity 41 0.044
104
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 40 0.044
105
CDQ001 Cauda Equina Syndrome 40 0.044
106
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 40 0.044
107
c PNT036 Pontocerebellar Hypoplasia, Type 6 40 0.044
108
HYP064 Hypogonadotropism 40 0.044
109
c PNT049 Pontocerebellar Hypoplasia, Type 2d 40 0.044
110
MTR007 Motor Peripheral Neuropathy 40 0.044
111
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 39 0.044
112
c HRD088 Hereditary Neuropathies 39 0.044
113
P CRB088 Cerebral Atrophy 39 0.044
114
c WRD032 Waardenburg Syndrome, Type 2a 39 0.044
115
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 39 0.044
116
BRC011 Brachial Plexus Neuropathy 39 0.044
117
ANS016 Anosmia 39 0.044
118
c MSC117 Muscular Dystrophy, Limb-Girdle, Type 1e 38 0.044
119
P AXN001 Axonal Neuropathy 38 0.044
120
c CHR504 Charcot-Marie-Tooth Disease, Type 4b3 38 0.044
121
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 38 0.044
122
c CHR420 Charcot-Marie-Tooth Disease, Type 4j 38 0.044
123
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 37 0.044
124
CHR073 Choreatic Disease 37 0.044
125
c BRN108 Branchiootic Syndrome 1 37 0.044
126
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 37 0.044
127
c MSC104 Muscular Dystrophy-Dystroglycanopathy , Type C, 1 37 0.044
128
MYP139 Myopathy, Proximal, and Ophthalmoplegia 37 0.044
129
c MSC108 Muscular Dystrophy-Dystroglycanopathy , Type C, 2 37 0.044
130
c MSC103 Muscular Dystrophy-Dystroglycanopathy , Type C, 4 37 0.044
131
c SPS109 Spastic Paraplegia 46, Autosomal Recessive 37 0.044
132
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 36 0.044
133
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 36 0.044
134
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 36 0.044
135
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 36 0.044
136
c WRD024 Waardenburg Syndrome, Type 4c 35 0.044
137
BRS004 Breast Angiosarcoma 35 0.044
138
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 35 0.044
139
c CHR642 Charcot-Marie-Tooth Disease, X-Linked Recessive, 3 35 0.044
140
FTD001 Foot Drop 35 0.044
141
AMY003 Amyotrophic Neuralgia 35 0.044
142
MLG005 Malignant Spindle Cell Melanoma 34 0.044
143
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 34 0.044
144
c SPS119 Spastic Paraplegia 55, Autosomal Recessive 34 0.044
145
c WRD031 Waardenburg Syndrome, Type 3 34 0.044
146
c CHR656 Charcot-Marie-Tooth Disease, Demyelinating, Type 1f 33 0.044
147
c ATS280 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h 33 0.044
148
DYS001 Dyskinetic Cerebral Palsy 33 0.044
149
c SPS071 Spastic Paraplegia 48, Autosomal Recessive 33 0.044
150
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 33 0.044
151
MST006 Mast Syndrome 33 0.044
152
c MSC057 Muscular Dystrophy, Limb-Girdle, Type 1f 33 0.044
153
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 33 0.044
154
c SPS137 Spastic Paraplegia 57, Autosomal Recessive 33 0.044
155
c MSC093 Muscular Dystrophy-Dystroglycanopathy , Type C, 3 32 0.044
156
c CHR351 Charcot-Marie-Tooth Disease, Axonal, Type 2n 32 0.044
157
c MSC098 Muscular Dystrophy-Dystroglycanopathy , Type C, 14 32 0.044
158
CLD014 Cole Disease 32 0.044
159
c CHR542 Charcot-Marie-Tooth Disease, Axonal, Type 2t 32 0.044
160
c WRD010 Waardenburg Syndrome Type 4 32 0.044
161
c MSC111 Muscular Dystrophy-Dystroglycanopathy , Type C, 7 31 0.044
162
c MSC100 Muscular Dystrophy-Dystroglycanopathy , Type C, 9 31 0.044
163
c MSC062 Muscular Dystrophy, Limb-Girdle, Type 2q 31 0.044
164
c CHR626 Charcot-Marie-Tooth Disease, Axonal, Type 2a1 31 0.044
165
P NRP059 Neuropathy, Hereditary Motor and Sensory, Type Via 31 0.044
166
c ATS297 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f 31 0.044
167
c PNT044 Pontocerebellar Hypoplasia, Type 2a 31 0.044
168
c CHR135 Charcot-Marie-Tooth Disease Type 2a 30 0.044
169
c MSC136 Muscular Dystrophy, Limb-Girdle, Type 2w 30 0.044
170
c CHR547 Charcot-Marie-Tooth Disease, Axonal, Type 2u 30 0.044
171
c ATS298 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b 29 0.044
172
c CHR608 Charcot-Marie-Tooth Disease, Axonal, Type 2p 29 0.044
173
c CHR657 Charcot-Marie-Tooth Disease, Axonal, Type 2j 29 0.044
174
c CHR545 Charcot-Marie-Tooth Disease, Axonal, Type 2h 29 0.044
175
c MSC095 Muscular Dystrophy, Limb-Girdle, Type 2r 29 0.044
176
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 29 0.044
177
c CHR650 Charcot-Marie-Tooth Disease, Axonal, Type 2b1 29 0.044
178
P DST101 Distal Hereditary Motor Neuropathies 28 0.044
179
ATX038 Ataxia and Polyneuropathy, Adult-Onset 28 0.044
180
c CHR489 Charcot-Marie-Tooth Disease, Axonal, Type 2q 28 0.044
181
c NRN037 Neuronopathy, Distal Hereditary Motor, Type Va 28 0.044
182
c ERL012 Early-Onset Glaucoma 27 0.044
183
c CHR671 Charcot-Marie-Tooth Disease, Axonal, Type 2r 27 0.044
184
c CHR641 Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 27 0.044
185
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 27 0.044
186
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 27 0.044
187
c CHR652 Charcot-Marie-Tooth Disease, Axonal, Type 2i 27 0.044
188
CCH001 Cochlear Disease 26 0.044
189
c CHR514 Charcot-Marie-Tooth Disease, Recessive Intermediate D 26 0.044
190
HYP213 Hypomelanotic Disorder 25 0.044
191
GNT018 Gianotti Crosti Syndrome 25 0.044
192
NRP009 Neuropathy, Hereditary Motor and Sensory, Okinawa Type 24 0.044
193
ALK024 Alkuraya-Kucinskas Syndrome 24 0.044
194
HTR005 Heterochromia Iridis 23 0.044
195
c CHR622 Charcot-Marie-Tooth Disease Type 2a2 23 0.044
196
c AMY022 Amyotrophic Lateral Sclerosis Type 5 22 0.044
197
CNG102 Congenital Hypomyelination Neuropathy 22 0.044
198
c CHR025 Charcot-Marie-Tooth Disease Intermediate Type 22 0.044
199
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 21 0.044
200
c ATS133 Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1g 21 0.044
201
PNT016 Pontoneocerebellar Hypoplasia 21 0.044
202
c DST030 Distal Hereditary Motor Neuropathy, Type V 20 0.044
203
c CHR115 Charcot-Marie-Tooth Neuropathy Type 2a 19 0.044
204
c CHR147 Charcot-Marie-Tooth Disease Type 2k 17 0.044
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