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Feingold syndrome type 2

ORPHA:391646 · Clinical subtype · Subtype of disorder

HPO 表現型（共 15 項）

Very frequent (99-80%)(5)

  • Abnormality of the skeletal systemHP:0000924
  • Intellectual disabilityHP:0001249
  • MicrocephalyHP:0000252
  • Neurodevelopmental delayHP:0012758
  • Short middle phalanx of fingerHP:0005819

Frequent (79-30%)(6)

  • Abnormal facial shapeHP:0001999
  • BrachydactylyHP:0001156
  • Jejunal atresiaHP:0005235
  • Short statureHP:0004322
  • Short thumbHP:0009778
  • Toe syndactylyHP:0001770

Occasional (29-5%)(4)

  • AnxietyHP:0000739
  • Atypical behaviorHP:0000708
  • Emotional labilityHP:0000712
  • Ventricular septal defectHP:0001629