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1 autosomal dominant Opitz syndrome
Medicine: ADOSУниверсальный русско-английский словарь > autosomal dominant Opitz syndrome
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2 синдром BBB
Medicine: G syndrome, Opitz G/BBB syndrome, autosomal dominant Opitz syndrome, 22q11. 2 deletion syndrome, hypertelorism-hypospadias syndrome, hypertelorism with esophageal abnormalities and hypospadias, Opitz BBB/G syndrome, Opitz BBB syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, X-linked Opitz syndrome -
3 синдром Опитца–Фриаса
Medicine: G syndrome, Opitz G/BBB syndrome, autosomal dominant Opitz syndrome, 22q11. 2 deletion syndrome, hypertelorism-hypospadias syndrome, hypertelorism with esophageal abnormalities and hypospadias, Opitz BBB/G syndrome, Opitz BBB syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, X-linked Opitz syndromeУниверсальный русско-английский словарь > синдром Опитца–Фриаса
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4 синдром гипоспадии–дисфагии
Medicine: G syndrome, Opitz G/BBB syndrome, autosomal dominant Opitz syndrome, 22q11. 2 deletion syndrome, hypertelorism-hypospadias syndrome, hypertelorism with esophageal abnormalities and hypospadias, Opitz BBB/G syndrome, Opitz BBB syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, X-linked Opitz syndromeУниверсальный русско-английский словарь > синдром гипоспадии–дисфагии
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5 телекант с сопутствующими аномалиями
Medicine: G syndrome, Opitz G/BBB syndrome, autosomal dominant Opitz syndrome, 22q11. 2 deletion syndrome, hypertelorism-hypospadias syndrome, hypertelorism with esophageal abnormalities and hypospadias, Opitz BBB/G syndrome, Opitz BBB syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, X-linked Opitz syndromeУниверсальный русско-английский словарь > телекант с сопутствующими аномалиями
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6 синдром Опитца
Medicine: G syndrome, autosomal dominant Opitz syndrome, 22q11. 2 deletion syndrome, hypertelorism-hypospadias syndrome, hypertelorism with esophageal abnormalities and hypospadias, Opitz BBB/G syndrome, Opitz BBB syndrome, Opitz-Frias syndrome, Opitz G syndrome, Opitz syndrome, X-linked Opitz syndrome -
7 велокардиофасциальный дефект
Medicine: cardiofacial syndrome, velocardiofacial syndrome, velo-cardio-facial syndrome, Shprintzen syndrome, Sedlackova syndrome, DiGeorge syndrome, deletion 22q11. 2 syndrome, conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, CATCH22, autosomal dominant Opitz G/BBB syndromeУниверсальный русско-английский словарь > велокардиофасциальный дефект
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8 синдром ДиДжорджи
Medicine: cardiofacial syndrome, velocardiofacial syndrome, velo-cardio-facial syndrome, Shprintzen syndrome, Sedlackova syndrome, DiGeorge syndrome, deletion 22q11. 2 syndrome, conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, CATCH22, autosomal dominant Opitz G/BBB syndrome -
9 синдром Такао
Medicine: cardiofacial syndrome, velocardiofacial syndrome, velo-cardio-facial syndrome, Shprintzen syndrome, Sedlackova syndrome, DiGeorge syndrome, deletion 22q11. 2 syndrome, conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, CATCH22, autosomal dominant Opitz G/BBB syndrome -
10 синдром Шпринтцена
Medicine: cardiofacial syndrome, velocardiofacial syndrome, velo-cardio-facial syndrome, Shprintzen syndrome, Sedlackova syndrome, DiGeorge syndrome, deletion 22q11. 2 syndrome, conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, CATCH22, autosomal dominant Opitz G/BBB syndromeУниверсальный русско-английский словарь > синдром Шпринтцена
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11 кардиофациальный синдром
Medicine: cardiofacial syndrome, velo-cardio-facial syndrome, Shprintzen syndrome, DiGeorge syndrome, Sedlackova syndrome, deletion 22q11. 2 syndrome, conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, CATCH22, autosomal dominant Opitz G/BBB syndromeУниверсальный русско-английский словарь > кардиофациальный синдром
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12 вело-кардио-фациальный синдром
Medicine: velocardiofacial syndrome (группа микроделеционных наследственных заболеваний, связанных с утратой участка 22 хромосомы (22q11)), deletion 22q11.2 syndrome, conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, CATCH22, autosomal dominant Opitz G/BBB syndromeУниверсальный русско-английский словарь > вело-кардио-фациальный синдром
См. также в других словарях:
Opitz syndrome — Opitz Frias syndrome an autosomal dominant syndrome consisting of hypertelorism and hernias, and in males hypospadias, cryptorchidism, and bifid scrotum. Cardiac anomalies, laryngotracheal malformations, imperforate anus, renal defects, lung… … Medical dictionary
Opitz — may refer to: Persons Martin Opitz, German poet Lucille Opitz, German speed skater Mark Opitz, Australian record producer Rudolf Opitz, German lithographer Simone Opitz, East German cross country skier Reinhard Opitz, German left wing… … Wikipedia
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
Syndrome, Brachmann-de Lange — A relatively common birth defect syndrome, also known as the de Lange syndrome, with multiple malformations and mental retardation of unknown origin. The syndrome is recognized by the presence of: Prenatal and postnatal growth retardation;… … Medical dictionary
Syndrome, Cornelia de Lange — A relatively common birth defect syndrome with multiple malformations and mental retardation of unknown origin that is recognized by the presence of: Prenatal and postnatal growth retardation; Delayed development and mental retardation;… … Medical dictionary
Syndrome, de Lange — A relatively common syndrome with multiple congenital malformations (birth defects) and mental retardation of unknown origin that is recognized by the presence of: Prenatal and postnatal growth retardation; Delayed development and mental… … Medical dictionary
Noonan syndrome — Classification and external resources A 12 year old female with Noonan syndrome. Typical webbed neck. Double structural curve with rib deformity. ICD 10 Q … Wikipedia
Robinow syndrome — Classification and external resources An infant exhibiting the facial features of Robinow syndrome. ICD 10 Q … Wikipedia
Branchio-oto-renal syndrome — Classification and external resources OMIM 113650 DiseasesDB 32599 MeSH … Wikipedia
Saethre-Chotzen syndrome — Classification and external resources OMIM 101400 DiseasesDB 29331 MeSH … Wikipedia
Nail–patella syndrome — Classification and external resources Nail of a patient with nail patella syndrome ICD 10 Q … Wikipedia
