/periventricular nodular heterotopia 6

periventricular nodular heterotopia 6

Rare Disease

MONDO:0014240

Also Known As

ERMARD periventricular nodular heterotopiaperiventricular nodular heterotopia 6periventricular nodular heterotopia caused by mutation in ERMARDperiventricular nodular heterotopia type 6PVNH6

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

ERMARD ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615544 ↗

GARD

GARD:15983 ↗

Related Diseases

heterotopia, periventricular, X-linked dominant

MONDO:0010233

Rare

periventricular heterotopia with microcephaly, autosomal recessive

MONDO:0011966

Rare

heterotopia, periventricular, associated with chromosome 5P anomalies

MONDO:0011967

Rare

chromosome 5Q14.3 deletion syndrome, distal

MONDO:0013031

Rare

periventricular nodular heterotopia 7

MONDO:0014966

Rare

periventricular nodular heterotopia 9

MONDO:0030061

Rare

← Back to All Diseases