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Search results for (2E)-Decenoyl-CoA

272 hits were found for (2E)-Decenoyl-CoA

# Family MCID Name MIFTS Score
1
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 9.972
2
c WRD033 Waardenburg Syndrome, Type 2e 51 7.550
3
c PNT034 Pontocerebellar Hypoplasia, Type 2e 47 5.788
4
c MSC176 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 34 5.414
5
c PSD092 Pseudohypoaldosteronism, Type Iie 45 4.863
6
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 51 4.370
7
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 56 3.794
8
c CNG412 Congenital Disorder of Glycosylation, Type Ii 52 3.775
9
GNY003 Guanylate Cyclase 2e, Pseudogene 14 2.249
10
c ART054 Arthrogryposis, Distal, Type 2e 12 2.227
11
P MSC005 Muscular Dystrophy 68 0.159
12
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.159
13
P ICH004 Ichthyosis 55 0.153
14
ICH002 Ichthyosis Bullosa of Siemens 44 0.153
15
P CHR071 Charcot-Marie-Tooth Disease 65 0.148
16
TTH006 Tooth Disease 47 0.148
17
KRT009 Keratosis 52 0.130
18
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 38 0.130
19
EPD002 Epidermolytic Hyperkeratosis 54 0.123
20
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.100
21
P TRC086 Trichohepatoenteric Syndrome 1 57 0.092
22
P NRP001 Neuropathy 57 0.092
23
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.092
24
P PRP019 Peripheral Nervous System Disease 64 0.082
25
THR013 Thoracic Outlet Syndrome 49 0.082
26
P QLT011 Qualitative or Quantitative Defects of Sarcoglycan 24 0.082
27
ANR007 Anorexia Nervosa 64 0.071
28
P ANR048 Aniridia 1 64 0.071
29
ACN002 Acanthosis Nigricans 62 0.071
30
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.071
31
HPT082 Hepatic Adenomas, Familial 40 0.071
32
ADP007 Adie Pupil 40 0.071
33
ATX010 Ataxia Neuropathy Spectrum 39 0.071
34
c CHR656 Charcot-Marie-Tooth Disease, Demyelinating, Type 1f 35 0.071
35
P ACT232 Acute Necrotizing Encephalopathy 28 0.071
36
HNM002 Hinman Syndrome 26 0.071
37
BLD137 Blood Group--Ahonen 17 0.071
38
P RTN008 Retinitis Pigmentosa 77 0.058
39
MSC157 Muscular Dystrophy, Duchenne Type 70 0.058
40
P LKM062 Leukemia, Acute Lymphoblastic 68 0.058
41
AND002 Androgen Insensitivity Syndrome 66 0.058
42
c BRN108 Branchiootic Syndrome 1 62 0.058
43
NRM005 Neuromuscular Disease 62 0.058
44
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.058
45
P SZR006 Seizure Disorder 59 0.058
46
VSL002 Visual Epilepsy 58 0.058
47
P AXN002 Axenfeld-Rieger Syndrome 58 0.058
48
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.058
49
P LYM031 Lymphocytic Leukemia 56 0.058
50
SNS003 Sensory Peripheral Neuropathy 56 0.058
51
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 56 0.058
52
P DRR001 Diarrhea 55 0.058
53
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.058
54
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 48 0.058
55
RTN023 Retinitis 46 0.058
56
NRR001 Neuroretinitis 46 0.058
57
HLX001 Helix Syndrome 46 0.058
58
NRN002 Neuronitis 37 0.058
59
P AXN001 Axonal Neuropathy 36 0.058
60
ALR002 Al-Raqad Syndrome 32 0.058
61
MYC088 Mycobacterium Avium Complex Infections 30 0.058
62
c BLD140 Blood Group, I System 29 0.058
63
c CHR676 Charcot-Marie-Tooth Disease, Dominant Intermediate G 24 0.058
64
AND005 Androgen Insensitivity Syndrome, Mild 20 0.058
65
ESP021 Esophageal Cancer 90 0.041
66
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.041
67
P ATX030 Ataxia-Telangiectasia 83 0.041
68
c HPT073 Hepatitis C Virus 74 0.041
69
c SPN225 Spondyloarthropathy 1 74 0.041
70
P EPL164 Epilepsy 73 0.041
71
HMN044 Human Immunodeficiency Virus Type 1 73 0.041
72
CRB037 Cerebral Palsy 69 0.041
73
WRN001 Werner Syndrome 68 0.041
74
P NRV007 Nervous System Disease 68 0.041
75
c HRD010 Hereditary Spastic Paraplegia 67 0.041
76
P LBR001 Leber Congenital Amaurosis 67 0.041
77
BRR014 Barrett Esophagus 67 0.041
78
P PRS038 Personality Disorder 66 0.041
79
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.041
80
P MTR014 Motor Neuron Disease 66 0.041
81
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.041
82
P DYS154 Dystonia 65 0.041
83
P ANG001 Angelman Syndrome 65 0.041
84
P HRS035 Hirschsprung Disease 1 65 0.041
85
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.041
86
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 64 0.041
87
P VNW001 Von Willebrand's Disease 64 0.041
88
P KLL001 Kallmann Syndrome 64 0.041
89
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.041
90
NRF007 Neurofibroma 63 0.041
91
P PSR002 Psoriasis 63 0.041
92
P MVM001 Movement Disease 63 0.041
93
PPL049 Papillon-Lefevre Syndrome 63 0.041
94
P ACR001 Aicardi-Goutieres Syndrome 63 0.041
95
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.041
96
MCR013 Microphthalmia 62 0.041
97
P MST009 Mastocytosis 62 0.041
98
P SNS001 Sensorineural Hearing Loss 62 0.041
99
P BCK002 Beckwith-Wiedemann Syndrome 62 0.041
100
P DST002 Distal Arthrogryposis 61 0.041
101
ACQ007 Acquired Immunodeficiency Syndrome 61 0.041
102
P BCL017 B-Cell Lymphoma 61 0.041
103
NTR005 Nutritional Deficiency Disease 61 0.041
104
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.041
105
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.041
106
ART001 Arterial Tortuosity Syndrome 60 0.041
107
WLL001 Williams-Beuren Syndrome 60 0.041
108
P WRD001 Waardenburg's Syndrome 60 0.041
109
c DWL002 Dowling-Degos Disease 1 59 0.041
110
EYD002 Eye Disease 59 0.041
111
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.041
112
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.041
113
c PTT056 Pituitary Adenoma 1, Multiple Types 59 0.041
114
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 0.041
115
WLF002 Wolf-Hirschhorn Syndrome 58 0.041
116
AGN016 Aging 58 0.041
117
LGS001 Legius Syndrome 57 0.041
118
PBL005 Piebald Trait 57 0.041
119
c WRD030 Waardenburg Syndrome, Type 1 57 0.041
120
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.041
121
P MCR010 Microcephaly 56 0.041
122
c SVR001 Severe Acute Respiratory Syndrome 56 0.041
123
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.041
124
DBT010 Diabetic Neuropathy 56 0.041
125
MYP139 Myopathy, Proximal, and Ophthalmoplegia 56 0.041
126
P LTR001 Lateral Sclerosis 56 0.041
127
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.041
128
c INT072 Intestinal Pseudo-Obstruction 55 0.041
129
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.041
130
TTZ003 Tietz Albinism-Deafness Syndrome 55 0.041
131
P ALP106 Alport Syndrome 1, X-Linked 55 0.041
132
P CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.041
133
P DYS193 Dystonia 11, Myoclonic 55 0.041
134
P TRM003 Tremor 55 0.041
135
P PLY019 Polyneuropathy 55 0.041
136
c CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 55 0.041
137
P HYP730 Hypogonadotropic Hypogonadism 54 0.041
138
PRP016 Paraplegia 54 0.041
139
P SJG002 Sjogren-Larsson Syndrome 54 0.041
140
P HML001 Hemolytic-Uremic Syndrome 54 0.041
141
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.041
142
P CNT004 Centronuclear Myopathy 53 0.041
143
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 53 0.041
144
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.041
145
c ALB020 Albinism, Oculocutaneous, Type Iii 53 0.041
146
SPS003 Spastic Diplegia 53 0.041
147
CHR629 Charcot-Marie-Tooth Disease and Deafness 53 0.041
148
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.041
149
DYS073 Dysphagia 52 0.041
150
CHR073 Choreatic Disease 52 0.041
151
DYS022 Dyschromatosis Symmetrica Hereditaria 52 0.041
152
P GNT009 Giant Axonal Neuropathy 52 0.041
153
P HYP077 Hypertrichosis 51 0.041
154
QDR001 Quadriplegia 51 0.041
155
BRN071 Brain Injury 51 0.041
156
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 51 0.041
157
HYP080 Hypogonadism 51 0.041
158
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 49 0.041
159
MYP136 Myopathy, Centronuclear, X-Linked 49 0.041
160
P OCL001 Ocular Albinism 48 0.041
161
ATN005 Autonomic Dysfunction 48 0.041
162
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 48 0.041
163
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.041
164
ALB002 Albinism 48 0.041
165
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.041
166
P HRD021 Hereditary Sensory Neuropathy 47 0.041
167
MGC001 Megacolon 47 0.041
168
c WRD032 Waardenburg Syndrome, Type 2a 47 0.041
169
P MYC033 Myoclonus 47 0.041
170
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 47 0.041
171
c WRD020 Waardenburg Syndrome, Type 4a 46 0.041
172
P HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 46 0.041
173
LCK001 Locked-in Syndrome 46 0.041
174
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.041
175
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 45 0.041
176
ANX004 Anoxia 44 0.041
177
c PNT049 Pontocerebellar Hypoplasia, Type 2d 44 0.041
178
ANC002 Anca-Associated Vasculitis 43 0.041
179
c PCH010 Pachyonychia Congenita 3 43 0.041
180
c WRD031 Waardenburg Syndrome, Type 3 43 0.041
181
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 43 0.041
182
P CRB088 Cerebral Atrophy 43 0.041
183
P DMY001 Demyelinating Polyneuropathy 43 0.041
184
c CHR420 Charcot-Marie-Tooth Disease, Type 4j 43 0.041
185
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 42 0.041
186
c WRD019 Waardenburg Syndrome, Type 4b 42 0.041
187
RDN001 Reading Disorder 42 0.041
188
CHR557 Chronic Intestinal Pseudoobstruction 41 0.041
189
CLD014 Cole Disease 41 0.041
190
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 41 0.041
191
c PNT036 Pontocerebellar Hypoplasia, Type 6 41 0.041
192
ALK024 Alkuraya-Kucinskas Syndrome 41 0.041
193
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 41 0.041
194
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 41 0.041
195
c GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 40 0.041
196
HYP064 Hypogonadotropism 40 0.041
197
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 40 0.041
198
BRS004 Breast Angiosarcoma 40 0.041
199
SPS004 Spastic Quadriplegia 39 0.041
200
MTR007 Motor Peripheral Neuropathy 39 0.041
201
P PNT019 Pontocerebellar Hypoplasia 39 0.041
202
CHR687 Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy 39 0.041
203
c CHR649 Charcot-Marie-Tooth Disease, Axonal, Type 2d 39 0.041
204
c HRD088 Hereditary Neuropathies 39 0.041
205
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 39 0.041
206
c WRD024 Waardenburg Syndrome, Type 4c 38 0.041
207
c SPS109 Spastic Paraplegia 46, Autosomal Recessive 38 0.041
208
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 37 0.041
209
MLG005 Malignant Spindle Cell Melanoma 37 0.041
210
c SPS071 Spastic Paraplegia 48, Autosomal Recessive 37 0.041
211
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 36 0.041
212
CHR178 Chromosomal Triplication 36 0.041
213
c CHR608 Charcot-Marie-Tooth Disease, Axonal, Type 2p 36 0.041
214
MST006 Mast Syndrome 36 0.041
215
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 36 0.041
216
c SPS137 Spastic Paraplegia 57, Autosomal Recessive 35 0.041
217
c CHR504 Charcot-Marie-Tooth Disease, Type 4b3 35 0.041
218
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 35 0.041
219
P NRP066 Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy 35 0.041
221
c CHR642 Charcot-Marie-Tooth Disease, X-Linked Recessive, 3 34 0.041
222
c CHR351 Charcot-Marie-Tooth Disease, Axonal, Type 2n 34 0.041
223
FTD001 Foot Drop 34 0.041
224
c SPN335 Spinocerebellar Ataxia Type 1 with Axonal Neuropathy 34 0.041
225
c CHR542 Charcot-Marie-Tooth Disease, Axonal, Type 2t 34 0.041
226
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.041
227
c SPS119 Spastic Paraplegia 55, Autosomal Recessive 33 0.041
228
DYS001 Dyskinetic Cerebral Palsy 33 0.041
229
c PNT044 Pontocerebellar Hypoplasia, Type 2a 33 0.041
230
c CHR671 Charcot-Marie-Tooth Disease, Axonal, Type 2r 33 0.041
231
c CHR657 Charcot-Marie-Tooth Disease, Axonal, Type 2j 33 0.041
232
c CHR650 Charcot-Marie-Tooth Disease, Axonal, Type 2b1 33 0.041
233
c ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 32 0.041
234
c CHR626 Charcot-Marie-Tooth Disease, Axonal, Type 2a1 32 0.041
235
CCH001 Cochlear Disease 31 0.041
236
CRB009 Cerebritis 31 0.041
237
MLN070 Melanoma-Astrocytoma Syndrome 31 0.041
238
c CHR489 Charcot-Marie-Tooth Disease, Axonal, Type 2q 31 0.041
239
AMY003 Amyotrophic Neuralgia 31 0.041
240
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 31 0.041
241
c CHR652 Charcot-Marie-Tooth Disease, Axonal, Type 2i 31 0.041
242
MTR087 Maternal Uniparental Disomy 30 0.041
243
NRP009 Neuropathy, Hereditary Motor and Sensory, Okinawa Type 30 0.041
244
c PNT046 Pontocerebellar Hypoplasia, Type 5 30 0.041
245
c WRD010 Waardenburg Syndrome Type 4 30 0.041
246
c ERL012 Early-Onset Glaucoma 29 0.041
247
DLT018 Dilution, Pigmentary 28 0.041
248
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.041
249
c AMY022 Amyotrophic Lateral Sclerosis Type 5 27 0.041
250
P PPL023 Pupil Disease 27 0.041
251
c CHR514 Charcot-Marie-Tooth Disease, Recessive Intermediate D 27 0.041
252
P ATS426 Autosomal Dominant Distal Hereditary Motor Neuronopathy 27 0.041
253
c CHR545 Charcot-Marie-Tooth Disease, Axonal, Type 2h 26 0.041
254
c CHR641 Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 26 0.041
255
c SPS092 Spastic Paraplegia 11 26 0.041
256
PNT016 Pontoneocerebellar Hypoplasia 25 0.041
257
c CHR135 Charcot-Marie-Tooth Disease Type 2a 25 0.041
258
HYP213 Hypomelanotic Disorder 25 0.041
259
GNT018 Gianotti Crosti Syndrome 24 0.041
260
c CHR025 Charcot-Marie-Tooth Disease Intermediate Type 24 0.041
261
c CHR115 Charcot-Marie-Tooth Neuropathy Type 2a 24 0.041
262
EXF002 Exfoliative Ichthyosis 23 0.041
263
ARG003 Argyll Robertson Pupil 22 0.041
264
HTR005 Heterochromia Iridis 21 0.041
265
c CHR622 Charcot-Marie-Tooth Disease Type 2a2 19 0.041
266
c CHR147 Charcot-Marie-Tooth Disease Type 2k 17 0.041
267
c ATS452 Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy 16 0.041
269
ABN004 Abnormal Pupillary Function 15 0.041
270
c MTR062 Maternal Uniparental Disomy of Chromosome 4 14 0.041
271
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.041
272
c AXN013 Axonal Hereditary Motor and Sensory Neuropathy 12 0.041
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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