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

Osteoporosis of bone 

m1 = Abeta Lipoproteinemia(Acanthocytosis)
autosomal recessive
m2 = Acatalasia autosomal recessive
M3 = Acute intermittent porphyria autosomal dominant
m4 = Adult amaurotic idiocy ( Kufs )
autosomal recessive 
m5 = Alkaptonuria autosomal recessive 
m6 = Alpha ketoadipic aciduria
m7 = Argininosuccinic aciduria(Hyperammonemia)
autosomal recessive
m8 = Beta aminoisobutyric aciduria autosomal recessive
m9 = Citrullinemia(Hyperammonemia)
autosomal recessive
m10 = Cystathioninemia
autosomal recessive
m11 = Deficiency of Glucose-6-phosphate dehydrogenase
(G-6-PD deficiency) X-linked recessive
m12 = Deficiency of pseudocholinesterase
autosomal recessive
m13 = Diabetes mellitus(Hyperglycemia,glycosuria)
autosomal recessive
M14 = Familial combined hyperlipidemia
autosomal dominant
m15 = Familial high-density lipoprotein disease (Tangier disease)
autosomal recessive
M16 = Familial hyperbetalipoproteinemia
(Essential familial hypercholesterolemia type II) autosomal dominant
m17 = Familial hyperchylomicronemia typeI (Lipoprotein lipase deficiency) autosomal recessive
M18 = Familial hypertriglyceridemia   autosomal dominant
m19 = Formiminoglutamic aciduria
m20 = Galactosemia autosomal recessive
m21 = Generalized gangliosidosis(GM1 gangliosidosis)
m22 = Globoid cell leukodystrophy(Krabbe's disease)
M23 = Glucoglycinuria  autosomal dominant
autosomal recessive
m24 = Glutaric aciduria
m25 = Glycinuria autosomal recessive
m26 = Glycogen storage type 0
m27 = Glycogen storage type I( Von Gierke's disease)
m28 = Glycogen storage type II ( Pompe)
m29 = Glycogen storage type III ( Cori Limit dextrinosis)
m30 = Glycogen storage type IV ( Andersen Amylopectinosis)
m31 = Glycogen storage type V ( Mc Ardle)
m32 = Glycogen storage type VI ( Hers)
m33 = Glycogen storage type VII
m34 = Glycogen storage type VIII
m35 = Glycogen storage type IXa
m36 = Glycogen storage type IXb
m37 = Glycogen storage type X
m38 = Glycogen storage type XI
m39 = Glycogen storage type XII
m40 = Glycolipid lipidosis(Fabry's disease)
X-linked recessive, autosomal recessive
M41,m41 = Hemochromatosis
autosomal dominant & recessive
m42 =Hepatic N-acetyl-transferase (Slow inactivators)
autosomal recessive
m43 = Hepatolenticular degeneration(Wilson's disease)
autosomal recessive
m44 = Hereditary disaccharide intolerance
autosomal recessive
m45 = Hereditary fructose intolerance & essential
fructosuria autosomal recessive
m46 = Hereditary lacctose intolerance
autosomal recessive
m47 = Hereditary orotic aciduria autosomal recessive 
m48 = Histidinemia autosomal recessive
m49 = Homocystinuria autosomal recessive
________________
Back      Next

Update since 10/09/50