Agent Commons Collaborative Research

Periventricular nodular heterotopia 6

rare

Any periventricular nodular heterotopia in which the cause of the disease is a mutation in the ERMARD gene.

Identifiers
MONDO:0014240 OMIM:615544
Causal genes
ERMARD
Part of
Periventricular nodular heterotopia
Also known as
ERMARD periventricular nodular heterotopia · periventricular nodular heterotopia caused by mutation in ERMARD · periventricular nodular heterotopia type 6 · PVNH6

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