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hydrocephalus, nonsyndromic, autosomal recessive 2

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any congenital hydrocephalus in which the cause of the disease is a mutation in the MPDZ gene.

Synonyms

  • HYC2
  • MPDZ congenital hydrocephalus
  • congenital hydrocephalus caused by mutation in MPDZ
  • hydrocephalus, congenital, 2, with or without brain or eye anomalies
  • hydrocephalus, nonsyndromic, autosomal recessive 2
  • hydrocephalus, nonsyndromic, autosomal recessive type 2HYC2
  • MPDZ congenital hydrocephalus
  • congenital hydrocephalus caused by mutation in MPDZ
  • hydrocephalus, congenital, 2, with or without brain or eye anomalies
  • hydrocephalus, nonsyndromic, autosomal recessive 2
  • hydrocephalus, nonsyndromic, autosomal recessive type 2
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