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

6 entries on 1 page. Showing entries 1 - 6.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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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
0000357039 Positional foot deformity, Failure to thrive in infancy, Neurodevelopmental delay, Abnormality of the face, Abnormal skull morphology, Posteriorly rotated ears, Prominent superficial veins, Hypotonia, Delayed speech and language development, Melanocytic nevus - - Unknown 03y - - - - Andreas Laner 00472230
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