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partial trisomy syndrome

См. также в других словарях:

  • Trisomy — ICD9 = ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D014314A trisomy is a form of aneuploidy with the presence of three copies, instead of the normal two, of a particular chromosome.cite web… …   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

  • Patau syndrome — Classification and external resources Chromosome 13 ICD 10 Q91.4 Q …   Wikipedia

  • Chromosome 5q deletion syndrome — Classification and external resources Photomicrograph of bone marrow showing abnormal mononuclear megakaryocytes typical of 5q syndrome ICD O: M …   Wikipedia

  • Edwards syndrome — Infobox Disease Name = Trisomy 18 Caption = Chromosome 18 DiseasesDB = 13378 ICD10 = ICD10|Q|91|0|q|90 ICD10|Q|91|3|q|90 ICD9 = ICD9|758.2 ICDO = OMIM = MedlinePlus = eMedicineSubj = ped eMedicineTopic = 652 MeshID = Trisomy 18 or Edwards… …   Wikipedia

  • Cat eye syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29864 ICD10 = ICD9 = ICDO = OMIM = 115470 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Cat Eye Syndrome is a very rare malformation involving Chromosome 22. The short arm (p) and a …   Wikipedia

  • Marshall-Smith syndrome — Discovered in 1971 (Marshall, Graham, Scott, Boner, Smith). Marshall Smith Syndrome is characterized by unusual accelerated skeletal maturation (usually starting before birth) and symptoms like conspicuous physical characteristics, respiratory… …   Wikipedia

  • Marshall–Smith syndrome — Marshall Smith syndrome Classification and external resources ICD 10 GroupMajor.minor ICD 9 xxx …   Wikipedia

  • Emanuel syndrome — Classification and external resources OMIM 609029 Derivative 22 syndrome, or der(22), is a rare disorder associated with multiple congenital anomalies, including profound mental retardation, preauricular skin tags or pits, and conotruncal heart… …   Wikipedia

  • Derivative 22 syndrome — Derivative 22 syndrome, or der(22), is a rare disorder associated with multiple congenital anomalies, including profound mental retardation, preauricular skin tags or pits, and conotruncal heart defects. It can occur in offspring of carriers of… …   Wikipedia

  • cat-eye syndrome — an association of coloboma of the iris and anal atresia; there may also be many other anomalies, including preauricular skin tags or fistulas, hypertelorism, congenital heart disease, skeletal abnormalities, and renal malformations. It is… …   Medical dictionary

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