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Metadata
ID HP:0012758
Name Neurodevelopmental delay
Parent Relationships

is_a Neurodevelopmental abnormality

Related Diseases

has phenotype

  • ethylmalonic encephalopathy
  • neurodevelopmental disorder with midbrain and hindbrain malformations
  • mitochondrial DNA depletion syndrome 14
  • developmental delay and seizures with or without movement abnormalities
  • cerebellar atrophy, visual impairment, and psychomotor retardation
  • intellectual disability-severe speech delay-mild dysmorphism syndrome
  • Pitt-Hopkins-like syndrome 2
  • mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
  • Kaufman oculocerebrofacial syndrome
  • combined oxidative phosphorylation deficiency 24
  • Tatton-Brown-Rahman syndrome
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