Focal Cortical Dysplasia, Type Ii (FCORD2)

Alias:

Focal Cortical Dysplasia of Taylor

Cortical Dysplasia of Taylor, Dysplasia Only

Cortical Dysplasia of Taylor

Fcord2

Fcdt

Fcd2

Cdt

Focal Cortical Dysplasia of Taylor Balloon Cell Type

Cortical Dysplasia of Taylor Without Balloon Cells

Focal Cortical Dysplasia, Taylor Balloon Cell Type

Cortical Dysplasia of Taylor with Balloon Cells

Focal Cortical Dysplasia of Taylor, Type Iib

Focal Cortical Dysplasia, Type Ii, Somatic

Isolated Focal Cortical Dysplasia Type Iib

Isolated Focal Cortical Dysplasia Type Iia

Isolated Focal Cortical Dysplasia Type Ii

Focal Cortical Dysplasia, Type Iia

Focal Cortical Dysplasia, Type Iib

Dysplasia, Cortical, Focal Type Ii

Isolated Focal Cortical Dysplasia

Focal Cortical Dysplasia Type 2

Focal Cortical Dysplasia 2

Epilepsy Due to Fcd

Fcd Type Iib

Fcd Type Iia

Fcd Iia

Fcd Iib

Fcord2a

Fcord2b

Cdtbc

Fcdbc

Cdtd

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Focal Cortical Dysplasia, Type Ii, also known as focal cortical dysplasia of taylor, is related to isolated focal cortical dysplasia type ii and epilepsy. An important gene associated with Focal Cortical Dysplasia, Type Ii is TSC2 (TSC Complex Subunit 2), and among its related pathways/superpathways are Prolactin Signaling and Akt Signaling. The drugs Temsirolimus and Sirolimus have been mentioned in the context of this disorder. Affiliated tissues include brain and cortex, and related phenotypes are seizure and abnormality of the nervous system

Related ID：

MALACARDS：FCL081

OMIM：607341

MESH：D001927