- Hanhart syndrome
- Han·hart syndrome (hahnґhahrt) [Ernst Hanhart, Swiss physician, 1891–1973] see under syndrome.
Medical dictionary. 2011.
Hanhart syndrome
Look at other dictionaries:
Hanhart syndrome — any of several syndromes of variable inheritance, characterized chiefly by severe micrognathia, high nose root, small eyelid fissures, low set ears, and variable absence of digits or limbs, usually below the elbow or knee … Medical dictionary
Richner Hanhart syndrome — Richner Hanhart syndrome, also called Richner syndrome or Hanhart syndrome, [Hanhart E (1950) Über die Kombination von Peromelia mit Mikrognathia, ein neues Syndrom beim Menschen, entsprechend der Akroteriasis congenita von Wriedt und Mohr beim… … Wikipedia
Richner-Hanhart syndrome — Richner Hanhart syndrome. См. синдром Рихнера Ханхарта. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
[syndrome]; Richner-Hanhart syndrome; right hand side; right heelstrike — Royal Hospital for Sick Children … Medical dictionary
Richner-Hanhart syndrome — Rich·ner Han·hart syndrome (rikґnər hahnґhahrt) [Hermann Richner, Swiss physician, 20th century; Ernst Hanhart, Swiss physician, 1891–1973] type II tyrosinemia … Medical dictionary
Richner-Hanhart syndrome — type II tyrosinemia … 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
Hanhart — Ernst, Swiss internist, 1891–1973. See H. syndrome … Medical dictionary
síndrome de Richner-Hanhart — Eng. Richner Hanhart syndrome Ver tirosinemia tipo II … Diccionario de oftalmología
Liste Des Maladies Génétiques À Gène Identifié — Ceci est la liste des maladies génétiques à gène identifié. Voir aussi la : liste des maladies génétiques à gène non identifié. Les maladies génétiques citées ici sont les maladies génétiques dont le gène est connu (Symbole + de MIM) ou dont … Wikipédia en Français
