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Heterotopia, periventricular, associated with chromosome 5P anomalies(PVNH3)

MedGen UID:: 374963
•Concept ID:: C1842562
•: Disease or Syndrome

Synonyms:	PERIVENTRICULAR NODULAR HETEROTOPIA 3; PVNH3

Monarch Initiative:	MONDO:0011967
OMIM®:	608098

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVPeriventricular nodular heterotopia
- CROGVChromosome 5Q14.3 deletion syndrome, distal
- CROGVHeterotopia, periventricular, associated with chromosome 5P anomalies
- CROGVHeterotopia, periventricular, X-linked dominant
- CROGVPeriventricular heterotopia with microcephaly, autosomal recessive

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Fetal anomaly
  - Congenital Systemic Disorder
    - Abnormality of the nervous system
      - Abnormality of neuronal migration
        Periventricular nodular heterotopia
        Heterotopia, periventricular, associated with chromosome 5P anomalies

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Heterotopia, periventricular, associated with chromosome 5P anomalies
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