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Home > List

Disease list

No. Id Disease Disease int Tissue/Cell line PubmedID Study design
121 135 Neurological - 0 Huntington disease - 0 cerebellar cortex 18082412 Patient study phenotype-control
122 137 Neurological - 0 Huntington disease - 0 cerebellar cortex 18082412 Cell culture study
123 522 Neurological - 0 Prion disease - 0 central nervous system 18987751 Patient study phenotype-control
124 157 Neuroblastoma - 256700 adrenal gland 17297439 Patient study phenotype-control
125 158 Neuroblastoma - 256700 SK-N-AS cell 17297439 Cell culture study
126 168 Neuroblastoma - 256700 neuroblastoma cell 17283129 Patient study phenotype-phenotype
127 170 Neuroblastoma - 256700 neuroblastoma cell 17283129 Patient study phenotype-phenotype
128 171 Neuroblastoma - 256700 neuroblastoma cell 17283129 Patient study phenotype-phenotype
129 172 Neuroblastoma - 256700 neuroblastoma cell 18504438 Patient study phenotype-phenotype
130 203 Neuroblastoma - 256700 neuroblastoma cell 17943719 Patient study phenotype-phenotype
131 393 Neuroblastoma - 256700 ganglion 17483472 Patient study phenotype-control
132 662 Neuroblastoma - 256700 20473924 Patient study phenotype-control
133 455 Nasopharyngeal carcinoma - 161550 nasopharynx 18390668 Patient study phenotype-control
134 614 Myotonic dystrophy - 160900 skeletal muscle 20487562 Patient study phenotype-control
135 312 Myopathy, nemaline, 3 - 161800 muscle 17942673 Patient study phenotype-control
136 178 Myocardial infarction heart 18723672 Patient study phenotype-control
137 180 Myocardial infarction heart 18723672 Patient study phenotype-control
138 592 Myocardial infarction myocardium 20029200 Patient study phenotype-control
139 593 Myocardial infarction myocardium 20029200 Patient study phenotype-control
140 598 Myocardial infarction myocardium 19460962 Not clearly defined
141 361 Myelofibrosis, idiopathic - 254450 granulocyte 17976522 Patient study phenotype-control
142 309 Muscular dystrophy, limb-girdle, type 2B - 253601 muscle 17942673 Patient study phenotype-control
143 308 Muscular dystrophy, limb-girdle, type 2A - 253600 muscle 17942673 Patient study phenotype-control
144 305 Muscular - 0 muscular dystrophy, facioscapulohumeral - 0 muscle 17942673 Patient study phenotype-control
145 313 Muscular - 0 Dermatomyositis - 0 muscle 17942673 Patient study phenotype-control
146 314 Muscular - 0 Polymyositis - 0 muscle 17942673 Patient study phenotype-control
147 323 Muscular - 0 Inclusion body myopathy - 0 muscle 17942673 Patient study phenotype-control
148 365 Muscular - 0 Uterine leiomyoma - 0 myoma cell 17243163 Patient study phenotype-control
149 368 Muscular - 0 Uterine leiomyoma - 0 myoma cell 17243163 Patient study phenotype-control
150 370 Muscular - 0 Uterine leiomyoma - 0 myoma cell 17243163 Patient study phenotype-control