orodigitofacial

orodigitofacial
Relating to the mouth, fingers, and face.

Medical dictionary. 2011.

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Look at other dictionaries:

  • orodigitofacial dysostosis — oral facial digital syndrome …   Medical dictionary

  • OFD1 — Klassifikation nach ICD 10 Q87.0 Angeborenes Fehlbildungssyndrom mit vorwiegender Beteiligung des Gesichtes …   Deutsch Wikipedia

  • Oral-fazial-digital-Syndrom 1 — Klassifikation nach ICD 10 Q87.0 Angeborenes Fehlbildungssyndrom mit vorwiegender Beteiligung des Gesichtes …   Deutsch Wikipedia

  • Oro-fazio-digitales Syndrom Typ 1 — Klassifikation nach ICD 10 Q87.0 Angeborenes Fehlbildungssyndrom mit vorwiegender Beteiligung des Gesichtes …   Deutsch Wikipedia

  • Papillon-Leage-Psaume-Syndrom — Klassifikation nach ICD 10 Q87.0 Angeborenes Fehlbildungssyndrom mit vorwiegender Beteiligung des Gesichtes …   Deutsch Wikipedia

  • dysostosis — SYN: dysosteogenesis. [dys + G. osteon, bone, + osis, condition] acrofacial d. mandibulofacial d. associated with malformations of the extremities such as defective radius and thumbs, and radioulnar synostosis. SEE ALSO: Treacher Collins syndrome …   Medical dictionary

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • Mohr syndrome — an autosomal recessive disorder characterized by brachydactyly, clinodactyly, polydactyly, syndactyly, and bilateral hallucal polysyndactyly; by cranial, facial, lingual, palatal, and mandibular anomalies; and by episodic neuromuscular… …   Medical dictionary

  • oral-facial-digital syndrome type I — a male lethal X linked dominant disorder characterized by camptodactyly, polydactyly, and syndactyly; by cranial, facial, lingual, and dental anomalies; and by mental retardation, familial trembling, alopecia, and seborrhea of the face and milia …   Medical dictionary

  • oral-facial-digital syndrome type III — an autosomal recessive disorder characterized by postaxial hexadactyly of the hands and feet, by ocular, lingual, and dental anomalies, and by profound mental retardation. Called also orodigitofacial dysostosis and orofaciodigital s., type III …   Medical dictionary

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