Phenotypes for disease #03912 (EEOC (encephalopathy, epileptic, childhood-onset (EEOC)), OMIM:615369)

7 entries on 1 page. Showing entries 1 - 7.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000027252 movement disorder; developmental epileptic encephalopathy; 2m-onset epilepsy; structural changes brain, atrophy, thinned corpus callosum; severe developmental delay; no speech - - Isolated (sporadic) - - 00y02m - - Hirotomo Saitsu 00033854
0000027253 movement disorder; developmental epileptic encephalopathy; 7d-onset epilepsy; structural changes brain, atrophy, altered (de)myelination; severe developmental delay; no speech - - Isolated (sporadic) - - 00y00m - - Hirotomo Saitsu 00033855
0000060493 Epileptic encephalopathy, childhood-onset (OMIM:615369) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080924
0000155278 Paroxymal opisthotonus, DD, early-onset intractable epilepsy, generalized tonic-clonic seizures, Status epilepticus, myoclonic seizures, delayed psychomotor development, hypotonia, opisthotonus, and dysmorphism. Refractory partial and secondary generalized tonic-clonic or myoclonic seizures since age of 6 m. Mild dysmorphism (wide-set eyes, depressed nasal bridge, short anteverted nose.) Normal ALP level. Normal brain MRI. No microcephaly, bone deformity or joint contracture. - Early onset epileptic encephalopathies (EOEE) Familial, X-linked - - 00y10m - - Philippe Campeau 00207501
0000155291 Paroxymal opisthotonus, DD, early-onset intractable epilepsy, generalized tonic-clonic seizures, delayed psychomotor development, hypotonia, opisthotonus, and dysmorphism. Refractory partial and secondary generalized tonic-clonic or myoclonic seizures since age of 6 months. Normal ALP levels. Mild dysmorphism with wide-set eyes, depressed nasal bridge, and short anteverted nose. No status epilepticus, myoclonic seizures. No microcephaly, bone deformity or joint contracture. - EOEE Familial, X-linked - - - - - Philippe Campeau 00207513
0000303348 Global severe neurodevelopmental delay. Hypotonia severe, cortical visual impairment, opisthotonus. Mild diffuse volume loss by MRI. - - - 00y10m - 00y10m - - Aguan Daniel Wei 00411273
0000303349 Global severe neurodevelopmental delay. Mild diffuse volume lost by MRI. - - - 01y07m 01y07m 01y07m - - Aguan Daniel Wei 00411274
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