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GENATLAS PHENOTYPE
last update : 10-09-2019
Symbol NDDRA
Location 19q13.32
Name neurodevelopmental disorder with renal anomalies
Corresponding gene DHX34
Main clinical features
  • facial dysmorphy, polydactyly, hypothyroidism, failure to thrive, renal anomalies (polycystic kidneys, solitary kidney)
  • developmental delay and/or intellectual disability
  • Genetic determination not applicable
    Function/system disorder kidney and urinary tract
    neurology
    mental retardation
    Type disease
    Remark(s)