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Ogden syndrome

ORPHA:276432 · Malformation syndrome · Disorder

HPO 表現型（共 41 項）

Frequent (79-30%)(11)

  • Aplasia/Hypoplasia of the eyebrowHP:0100840
  • Broad halluxHP:0010055
  • Cerebral atrophyHP:0002059
  • Delayed cranial suture closureHP:0000270
  • Excessive daytime somnolenceHP:0001262
  • Fine hairHP:0002213
  • Generalized hypotoniaHP:0001290
  • Global developmental delayHP:0001263
  • Postnatal growth retardationHP:0008897
  • ScoliosisHP:0002650
  • TorticollisHP:0000473

Occasional (29-5%)(30)

  • Abnormal forehead morphologyHP:0000290
  • Abnormal head movementsHP:0002457
  • ArrhythmiaHP:0011675
  • Atypical behaviorHP:0000708
  • Autistic behaviorHP:0000729
  • Capillary malformationHP:0025104
  • Cardiogenic shockHP:0030149
  • Coarse facial featuresHP:0000280
  • CryptorchidismHP:0000028
  • Cutis laxaHP:0000973
  • Delayed gross motor developmentHP:0002194
  • Downslanted palpebral fissuresHP:0000494
  • Enlarged narisHP:0009931
  • Everted upper lip vermilionHP:0010803
  • Frontal bossingHP:0002007
  • High, narrow palateHP:0002705
  • HypertoniaHP:0001276
  • Inguinal herniaHP:0000023
  • LethargyHP:0001254
  • Low-set earsHP:0000369
  • MacrotiaHP:0000400
  • MicroretrognathiaHP:0000308
  • Narrow foreheadHP:0000341
  • ProptosisHP:0000520
  • Pulmonary artery stenosisHP:0004415
  • Short columellaHP:0002000
  • Shuffling gaitHP:0002362
  • Underdeveloped nasal alaeHP:0000430
  • Ventricular septal defectHP:0001629
  • VentriculomegalyHP:0002119