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heterotopia, periventricular, X-linked dominant

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Uniprot Description A developmental disorder characterized by the presence of periventricular nodules of cerebral gray matter, resulting from a failure of neurons to migrate normally from the lateral ventricular proliferative zone, where they are formed, to the cerebral cortex. PVNH1 is an X-linked dominant form. Heterozygous females have normal intelligence but suffer from seizures and various manifestations outside the central nervous system, especially related to the vascular system. Hemizygous affected males die in the prenatal or perinatal period.
Mondo Term and Equivalent IDs
MONDO:0010233:  heterotopia, periventricular, X-linked dominant
GARD:0007371: 
SCTID:448227009: