Goldenhar syndrome (Q769988)

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A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch.
  • Facio-auriculo-vertebral spectrum (disorder)
  • First AND second branchial arch syndrome
  • First arch syndrome (disorder)
  • HEMIFACIAL MICROSOMIA
  • OAV (oculoauriculovertebral) dysplasia
  • Otomandibular dysostosis (disorder)
  • First arch syndrome
  • Facio-auriculo-vertebral spectrum
  • Otomandibular dysostosis
  • Facioauriculovertebral dysplasia
  • Expanded spectrum of hemifacial microsomia
  • Oculoauriculovertebral dysplasia
  • Goldenhar Syndrome
  • Fav Sequence
  • Oculoauriculovertebral syndrome
  • Expanded spectrum hemifacial microsomia
  • Oculoauriculovertebral Spectrum
  • HFM
  • OAVS
  • Oav Dysplasia
  • HEMIFACIAL MICROSOMIA; HFM
  • Facioauriculovertebral Sequence
  • OAV
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Language Label Description Also known as
English
Goldenhar syndrome
A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch.
  • Facio-auriculo-vertebral spectrum (disorder)
  • First AND second branchial arch syndrome
  • First arch syndrome (disorder)
  • HEMIFACIAL MICROSOMIA
  • OAV (oculoauriculovertebral) dysplasia
  • Otomandibular dysostosis (disorder)
  • First arch syndrome
  • Facio-auriculo-vertebral spectrum
  • Otomandibular dysostosis
  • Facioauriculovertebral dysplasia
  • Expanded spectrum of hemifacial microsomia
  • Oculoauriculovertebral dysplasia
  • Goldenhar Syndrome
  • Fav Sequence
  • Oculoauriculovertebral syndrome
  • Expanded spectrum hemifacial microsomia
  • Oculoauriculovertebral Spectrum
  • HFM
  • OAVS
  • Oav Dysplasia
  • HEMIFACIAL MICROSOMIA; HFM
  • Facioauriculovertebral Sequence
  • OAV

Statements

Goldenhar syndrome
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Identifiers

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