Phenotypes for disease #02894 (CDCBM7 (dysplasia, cortical, complex, with other brain malformations, type 7 (CDCBM-7, polymicrogyria, asymmetric)), OMIM:610031)

9 entries on 1 page. Showing entries 1 - 9.
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AscendingPhenotype ID     

Phenotype details     

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0000078647 cerebellar dysplasia;Cerebellar vermis hypoplasia;Agenesis of corpus callosum; Abnormality of the basal ganglia; Polymicrogyria; Schizencephaly; Abnormality of the cranial nerves;neurodevelopmental delay;Spastic tetraparesis;intellectual disability,severe;ptosis;strabismus;Complex focal seizures - - Isolated (sporadic) - - - - - Enza Maria Valente 00100447
0000078648 Dysgenesis of the cerebellar vermis;Hypoplasia of the pons; Partial agenesis of the corpus callosum;Abnormality of the basal ganglia, polymicrogyria;neurodevelopmental delay;Congenital microcephaly; Focal seizures;Facial dysmorphisms - - Isolated (sporadic) - - - - - Enza Maria Valente 00100448
0000078649 Cerebellar dysplasia;Dysgenesis of the cerebellar vermis;Hypoplasia of the pons;Dysgenesis of corpus callosum;Anomaly of the basal ganglia; Perisylvian polymicrogyria; Congenital microcephaly - - Isolated (sporadic) - - - - - Enza Maria Valente 00100449
0000078650 Abnormality of the pons; Dysplastic corpus callosum; Abnormality of the basal ganglia; Polymicrogyria;Schizencephaly;neurodevelopmental delay;spastic tetraparesis;intellectual disability,severe;frequent vomiting - - Isolated (sporadic) - - - - - Enza Maria Valente 00100450
0000078651 Cerebellar vermis hypoplasia;Hypoplasia of the pons;Agenesis of corpus callosum; Abnormality of the basal ganglia; Perisylvian polymicrogyria;Hypoplasia of the optic nerve;Neurodevelopmental delay;Generalized hypotonia;Intellectual disability,severe;Congenital microcephaly;Congenital bilateral ptosis;Strabismus; Optic atrophy;Blindness;Epilepsy;Facial dysmorphisms - - Isolated (sporadic) - - - - - Enza Maria Valente 00100451
0000078699 Cerebellar vermis hypoplasia;Hypoplasia of the pons;Agenesis of corpus callosum;Abnormality of the basal ganglia;Simplified gyral pattern; Neurodevelopmental delay;Hypotonia;Congenital microcephaly;Optic nerve hypoplasia;Seizures;Facial dysmorphisms - - Isolated (sporadic) - - - - - Enza Maria Valente 00100452
0000078708 Cerebellar dysplasia;Hypoplasia of the pons;Thin corpus callosum;Abnormality of the basal ganglia;Neurodevelopmental delay;Spastic hemiparesis;Intellectual disability;Congenital microcephaly;Bilateral - - Isolated (sporadic) - - - - - Enza Maria Valente 00100453
0000078709 Cerebellar dysplasia;Hypoplasia of the pons;Abnormality of the basal ganglia;Neurodevelopmental delay;Spastic tetraparesis;Intellectual disability, severe;Congenital microcephaly;Optic nerve hypoplasia;Optic nerve atrophy;West syndrome;Thoracolumbar scoliosis - - Isolated (sporadic) - - - - - Enza Maria Valente 00100454
0000286634 prenatal ultrasound abnormalities: Abnormality of the septum pellucidum, Dilation of lateral ventricles, Cerebellar hypoplasia, Abnormal cerebral morphology 0y - Isolated (sporadic) - - - - - Andreas Laner 00393393
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