Phenotypes for disease #00183 (DEE7 (encephalopathy, developmental and epileptic, type 7), OMIM:613720)

19 entries on 1 page. Showing entries 1 - 19.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Owner     

Individual ID     
0000041475 - - - Unknown - - - - - NeuroMeGen 00054788
0000041476 - - - Unknown - - - - - NeuroMeGen 00054821
0000041477 - - - Unknown - - - - - NeuroMeGen 00054822
0000041478 - - - Unknown - - - - - NeuroMeGen 00054823
0000041479 - - - Unknown - - - - - NeuroMeGen 00054824
0000041480 - - - Unknown - - - - - NeuroMeGen 00054825
0000041481 - - - Unknown - - - - - NeuroMeGen 00054826
0000041482 - - - Unknown - - - - - NeuroMeGen 00054827
0000041483 - - - Unknown - - - - - NeuroMeGen 00054828
0000041484 - - - Unknown - - - - - NeuroMeGen 00054829
0000060406 Epileptic encephalopathy, early infantile, 7 (OMIM:613720) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080837
0000070607 profound IDD, epileptic encephalopathy, hypotonia, dysautonomia, microcephaly; CSF GABA free 0.007 umol/L (reference range: 0.017- 0.067) CSF GABA total 4.300 umol/L (reference range: 4.2-13.4) low CSF GABA, mitochondrial complex I and II deficiency - - Familial, autosomal dominant - - - - - Johan den Dunnen 00092271
0000087491 Developmental delay, hypotonia, seizures during first year of life - - Isolated (sporadic) - - - - - Bernt Popp 00111406
0000257304 Developmental delay, seizures, hypotonia, microcephaly - - Familial, autosomal dominant - - - - - Anju Shukla 00361907
0000257617 Epileptic encephalopathy with neonatal seizures from day 1, suspected Otahara syndrome, severe combined developmental delay, marked muscular hypotonia 0y - Unknown - - - - - Andreas Laner 00362203
0000272296 Autism, Autistic behavior, Seizure, Global developmental delay, Abnormal nervous system physiology, Neurodevelopmental delay - 5y Unknown - - - - - Andreas Laner 00377115
0000296423 Behavioral abnormality, Stereotypy, Hypotonia, Delayed speech and language development, Global developmental delay, Poor fine motor coordination - - Unknown 07y - - - - Andreas Laner 00403727
0000323533 Seizure, Motor delay, Infantile onset - - Unknown 00y04m - - - - Andreas Laner 00432970
0000350382 - - - Unknown - - - - - Min Peng 00464343
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