McLeod phenotype syndrome
Look at other dictionaries:
McLeod 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 … Medical dictionary
Syndrome de mcleod — Autre nom {{{Autre nom}}} Référence MIM 3 … Wikipédia en Français
Syndrome de McLeod — Référence MIM 314850 Transmission Récessive à l X Chromosome Xp21.2 p21.1 Gène XK Mutation Ponctuelle … Wikipédia en Français
McLeod 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 … Wikipedia
McLeod 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… … Medical dictionary
Androgen 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 … Wikipedia
Partial androgen 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 … Wikipedia
Rett syndrome — Classification and external resources ICD 10 F84.2 ICD 9 330.8 … Wikipedia
Fragile X syndrome — Classification and external resources Location of FMR1 gene ICD 10 Q99.2 … Wikipedia
Lujan-Fryns syndrome — Lujan–Fryns syndrome Classification and external resources Lujan–Fryns syndrome in a young adult male, with features that include a long, narrow face and recessed chin. ICD 10 F … Wikipedia
