Phenotypes for disease #05802 (DEE42;EIEE42 (encephalopathy, developmental and epileptic, type 42), OMIM:617106)

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000247213 - - (+) Autism,(+) Autistic behavior,(+) Seizure, (+) Rolando Focus in EEG Unknown - - - - Andreas Laner 00329009
0000270480 - - (+) Seizure,(+) Abnormal nervous system physiology Familial, autosomal dominant - 00y09m - - Andreas Laner 00375268
0000271542 - - Strabismus, Abnormal conjugate eye movement, Delayed speech and language development, Intellectual disability, Ataxia, Abnormal cerebellum morphology, Absent speech, Abnormality of coordination, Abnormality of higher mental function, Enlarged cerebellum, Neurodevelopmental abnormality Unknown - 07y - - Andreas Laner 00376334
0000274641 - Infantile epileptic encephalopathy type 42 DD; ID; Hypotonia; seizures (Neurological) Familial - - - - LOVD 00380788
0000290697 - - Seizure, onset 9 month; Familial 06y - - - Andreas Laner 00397574
0000350525 - - Hearing impairment, Strabismus, Delayed speech and language development, Hypotonia, Global developmental delay, Delayed gross motor development, Developmental stagnation Unknown 02y - - - Andreas Laner 00464525
0000351792 - - - Isolated (sporadic) 26 27 - - Mario Benvenuto 00466428
Legend   How to query  


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