mcleod syndrome
1McLeod syndrome — McLeod syndrome. См. синдром Мак Леода. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …
2McLeod syndrome — This article is about the genetic disease of the blood, not MacLeod s syndrome (the lung disease). McLeod syndrome Classification and external resources OMIM 314850 DiseasesDB 29708 …
3McLeod syndrome — a syndrome seen in some individuals having the McLeod phenotype of blood, characterized by mild hemolytic anemia with acanthocytes, elevated serum creatinine phosphokinase, and sometimes muscle wasting and neurological defects. A few cases have… …
4Syndrome de mcleod — Autre nom {{{Autre nom}}} Référence MIM 3 …
5McLeod phenotype — a rare blood phenotype with X linked inheritance in which several antigens of the Kell blood group are weakly expressed; affected individuals sometimes have an anemic condition called McLeod syndrome …
6Syndrome de McLeod — Référence MIM 314850 Transmission Récessive à l X Chromosome Xp21.2 p21.1 Gène XK Mutation Ponctuelle …
7McLeod phenotype syndrome — Mc·Leod phenotype, syndrome (mə kloudґ) [McLeod, surname of the propositus first observed in 1961] see under phenotype and syndrome …
8Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …
9Fragile X syndrome — Classification and external resources Location of FMR1 gene ICD 10 Q99.2 …
10Rett syndrome — Classification and external resources ICD 10 F84.2 ICD 9 330.8 …
