Phenotypes for disease #03404 (DEE11 (encephalopathy, developmental and epileptic, type 11), OMIM:613721)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060655 Epileptic encephalopathy, early infantile, 11 (OMIM:613721) - - Isolated (sporadic) - - - - - Daniel Trujillano 00081086
0000274792 Bilateral tonic-clonic seizure, Neonatal seizure, Neonatal epileptic spasm 04d - Isolated (sporadic) - - - - - Andreas Laner 00380939
0000308437 Macrocephaly HP:0000256 Ventriculomegaly HP:0002119 Supraventricular tachycardia HP:0004755 Cardiomegaly HP:0001640 Decreased body weight HP:0004325 Simplified gyral pattern HP:0009879 Low-set ears HP:0000369 Blepharophimosis HP:0000581 Epicanthus HP:0000286 Hypertelorism HP:0000316 Retrognathia HP:0000278 Hypotonia HP:0001252 Seizure HP:0001250 Fever HP:0001945 Hyponatremia HP:0002902 Hypoglycemia HP:0001943 Anemia HP:0001903 supraventricular tachyarrhythmias (SVT) DEE11 Isolated (sporadic) - - - - - Edoardo Errichiello 00416926
0000315812 Dystonia, Intellectual disability, mild, Ventricular septal defect, Lower limb spasticity, Aganglionosis of the small intestine, Arm dystonia - - Unknown 12y - - - - Andreas Laner 00424614
0000319006 Focal tonic seizure, Neurodevelopmental delay - - Unknown 02y - - - - Andreas Laner 00428060
0000326593 Severe global developmental delay, Microcephaly, Hypertelorism, Long palpebral fissure - - Unknown 02y - - - - Andreas Laner 00436412
0000351261 Neurodevelopmental delay, Motor delay, Gait ataxia, Absent speech, EEG abnormality, Neurodegeneration - - Isolated (sporadic) 02y - - - - Andreas Laner 00465814
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