Phenotypes for disease #04665 (MAE (epilepsy, myoclonic-atonic (MAE)), OMIM:616421)

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000300208 Seizure, Seizure precipitated by febrile infection, EEG abnormality, Hyperhidrosis, Nausea and vomiting, Generalized non-motor (absence) seizure, Myoclonic seizure Epilepsy - Familial, autosomal dominant - - - - - Andreas Laner 00408080
0000322432 Global developmental delay, Generalized non-motor (absence) seizure - - Unknown 06y - - - - Andreas Laner 00431864
0000322433 Generalized non-motor (absence) seizure, Seizure, Generalized myoclonic-atonic seizure, Expressive language delay, Receptive language delay, EEG abnormality, Neurodevelopmental delay - - Unknown 06y - - - - Andreas Laner 00431864
0000325349 (+) Pectus excavatum,(+) Seizure,(+) Absent speech,(+) Scoliosis,(+) Neurodevelopmental delay - - Isolated (sporadic) 24y - - - - Andreas Laner 00435117
0000337057 Neurodevelopmental delay, Intellectual disability, Autistic behavior - - Isolated (sporadic) 00y08m - - - - Andreas Laner 00447861
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.