oculoauricular syndrome (Q22030614)

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syndrome characterized by microcornea, microphthalmia, anterior-segment dysgenesis, cataract, coloboma of various parts of the eye, abnormalities of the retinal pigment epithelium, and rod-cone dystrophy and a particular cleft ear lobule
  • OCULOAURICULAR SYNDROME; OCACS
  • OCACS
  • Oculoauricular syndrome, Schorderet type
  • OCULOAURICULAR SYNDROME
  • Schorderet-Munier-Franceschetti Syndrome
  • Microphthalmia, Microcornea, Anterior Segment Dysgenesis, Cataract, Ocular Coloboma, Retinal Pigment Epithelium Abnormalities, Rod-Cone Dystrophy, and Anomalies of the External Ear
  • Oculoauricular syndrome
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English
oculoauricular syndrome
syndrome characterized by microcornea, microphthalmia, anterior-segment dysgenesis, cataract, coloboma of various parts of the eye, abnormalities of the retinal pigment epithelium, and rod-cone dystrophy and a particular cleft ear lobule
  • OCULOAURICULAR SYNDROME; OCACS
  • OCACS
  • Oculoauricular syndrome, Schorderet type
  • OCULOAURICULAR SYNDROME
  • Schorderet-Munier-Franceschetti Syndrome
  • Microphthalmia, Microcornea, Anterior Segment Dysgenesis, Cataract, Ocular Coloboma, Retinal Pigment Epithelium Abnormalities, Rod-Cone Dystrophy, and Anomalies of the External Ear
  • Oculoauricular syndrome

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