Image:Autorecessive.jpg

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This image is a work of the National Institutes of Health, part of the United States Department of Health and Human Services. As a work of the U.S. federal government, the image is in the public domain.

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(All user names refer to en.wikipedia)

• 2006-07-23 07:32 Apers0n 307×396×8 (69435 bytes) == Summary == {{Information |Description=Autosomal recessive inheritance. |Source=http://ghr.nlm.nih.gov/handbook/illustrations |Date= |Author=ghr.nlm.nih.gov |Permission=This image is a work of the National Institutes of Health, part of the United Sta

• Lafora disease
• Polycystic kidney disease
• Cystic fibrosis
• Dominance relationship
• Haemochromatosis
• Abetalipoproteinemia
• Cenani Lenz syndactylism
• Adducted thumb syndrome
• Donohue syndrome
• Methemoglobinemia
• Thalassemia
• Von Willebrand disease
• Weissenbacher-Zweymüller syndrome
• Werner syndrome
• Familial Mediterranean fever
• Mucopolysaccharidosis
• Propionic acidemia
• Medium-chain acyl-coenzyme A dehydrogenase deficiency
• Waardenburg syndrome
• Ichthyosis lamellaris
• Situs inversus
• Adenosine deaminase deficiency
• Usher syndrome
• Alpha-mannosidosis
• Glycogen storage disease type II
• Gunther's disease
• ICF syndrome
• Xeroderma pigmentosum
• Ellis-van Creveld syndrome
• Diastrophic dysplasia
• Atelosteogenesis, type II
• Cockayne syndrome
• Jervell and Lange-Nielsen syndrome
• Abderhalden-Kaufmann-Lignac syndrome
• Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
• Trimethylaminuria
• Glycogen storage disease type I
• Isovaleric acidemia
• Maple syrup urine disease
• Cystinosis
• Smith-Lemli-Opitz syndrome
• Holocarboxylase synthetase deficiency
• Beta-ketothiolase deficiency
• Gitelman syndrome
• Tyrosinemia
• Meleda disease
• Batten disease
• Metachromatic leukodystrophy
• Omenn syndrome
• Spinocerebellar ataxia
• Shwachman-Diamond syndrome
• Carnitine palmitoyltransferase I deficiency
• Carnitine palmitoyltransferase II deficiency
• GM2-gangliosidosis, AB variant
• Salla disease
• Giant axonal neuropathy
• Carnitine-acylcarnitine translocase deficiency
• Mitochondrial trifunctional protein deficiency
• Very long-chain acyl-coenzyme A dehydrogenase deficiency
• Lysinuric protein intolerance
• Fraser syndrome
• Leukocyte adhesion deficiency
• Carpenter syndrome
• Dubin-Johnson syndrome
• Glycogen storage disease type III
• Sugarman syndrome
• Behr's syndrome
• Biotinidase deficiency
• Pseudoxanthoma elasticum
• Wolman disease
• Mucolipidosis
• Chondrodystrophy
• Werdnig-Hoffman disease
• Walker-Warburg syndrome
• Aceruloplasminemia
• Tetrahydrobiopterin deficiency
• Glutaric acidemia type 2
• Bernard-Soulier syndrome
• Fountain syndrome
• Impossible syndrome
• 2-Hydroxyglutaric aciduria
• Malonyl-CoA decarboxylase deficiency
• Short-chain acyl-coenzyme A dehydrogenase deficiency
• D-Glyceric acidemia
• Recessive multiple epiphyseal dysplasia
• Progressive familial intrahepatic cholestasis
• Galloway Mowat syndrome
• Acrodermatitis enteropathica
• Fumarase deficiency
• Lucey-Driscoll syndrome
• Richner Hanhart syndrome
• Histidinemia
• Succinic semialdehyde dehydrogenase deficiency
• N-Acetylglutamate synthase deficiency
• Tangier disease
• Fucosidosis
• Mucolipidosis type IV
• Wikipedia talk:WikiProject Medical Genetics/Guidelines
• Isobutyryl-coenzyme A dehydrogenase deficiency
• Dihydropyrimidine dehydrogenase deficiency