Preface

Jarind's Letters

Sims'Letters

Genetic Lists

Prevention

Letters of Signs

Genetic Lists of Abnormal Genes ( Lists of Sims' Letters)

 

M = In born error of metabolism

Mucopolysaccharidoses

m50 = Hydroxykynureninuria autosomal recessive
m51 = Hydroxyprolinemia autosomal recessive
M52 = Hyperlipidemia(Broad beta disease type III) autosomal dominant
m53 = Hyperlysinemia autosomal recessive 
m54 = Hyperornithinemia(Hyperammonemia)
m55 = Hyperoxaluria autosomal recessive
m56 = Hyperprolinemia type I autosomal recessive
m57 = Hyperprolinemia type II autosomal recessive
m58 = Hyperuric aciduria(Lesch-Nyhan syndrome)
X-linked recessive
M59 = Hyperuricemia autosomal dominant
m60 = Hypervalinemia autosomal recessive
m61 = Hypophosphatasia autosomal recessive
m62 = Idiopathic spontaneous hypoglycemia
autosomal recessive
m63 = Infantile amaurotic idiocy(GM2 gangliosidosis,Tay-Sachs disease)
autosomal recessive
m64 = Infantile cerebroside lipidosis (Gaucher's disease)
autosomal recessive
m65 = Isovaleric acidemia autosomal recessive
m66 = Juvenile cerebral atrophy autosomal recessive
( Juvenile amaurotic idiocy,Vogt-Spielmeyer disease )
m67 = Juvenile GM2 gangliosidosis autosomal recessive
m68 = Late infantile GM1 gangliosidosis
m69 = Lipochondrodystrophy(Gargoylism) autosomal recessive
M70 = Malignant  Hyperthermia autosomal dominant
m71 = Maple syrup urine disease autosomal recessive
m72 = Methyl beta hydroxybutyric aciduria
m73 = Methyl crotonyl glycinuria autosomal recessive
m74 = Methyl malonic aciduria(Propionate metabolism)
autosomal recessive
m75 = Monosaccharide malabsorption autosomal recessive
m76 = Mucopolysaccharidosis type IH ( Hurler 's disease)
autosomal recessive
m77 = Mucopolysaccharidosis type IS ( Scheie 's disease)
autosomal recessive
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Update since 10/09/50