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
________________
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Dr.Jarind B. Sriraumpuch |
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Update since 10/09/50