File:Autorecessive.svg

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current | 19:06, 18 September 2023 | ![]() | 1,350 × 1,580 (3 KB) | wikimediacommons>Puck04 | remake (by hand); path text --> <text> |
File usage
The following 78 pages use this file:
- Abetalipoproteinemia
- Acheiropodia
- Adducted thumb syndrome
- Alpha-mannosidosis
- Aminolevulinic acid dehydratase deficiency porphyria
- Antley–Bixler syndrome
- Atransferrinemia
- Autosomal recessive polycystic kidney disease
- Batten disease
- Beta-ketothiolase deficiency
- Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
- Canavan disease
- Carnitine-acylcarnitine translocase deficiency
- Carnitine palmitoyltransferase II deficiency
- Carnitine palmitoyltransferase I deficiency
- Carnosinemia
- Carpenter syndrome
- Cystic fibrosis
- Cystinosis
- Donohue syndrome
- Dubin–Johnson syndrome
- Fraser syndrome
- Fumarase deficiency
- GM2-gangliosidosis, AB variant
- Gerodermia osteodysplastica
- Giant axonal neuropathy
- Gitelman syndrome
- Glutathione synthetase deficiency
- Glycogen storage disease type III
- Harding ataxia
- Hartnup disease
- Histidinemia
- Holocarboxylase synthetase deficiency
- Hyperprolinemia
- Hypertryptophanemia
- Juvenile primary lateral sclerosis
- Lafora disease
- Laron syndrome
- Leukodystrophy
- Lowry-Wood syndrome
- Lubani Al Saleh Teebi syndrome
- Lucey–Driscoll syndrome
- Lysinuric protein intolerance
- Lysosomal acid lipase deficiency
- Mendelian traits in humans
- Methemoglobinemia
- Mevalonate kinase deficiency
- Mitochondrial trifunctional protein deficiency
- Mucolipidosis type IV
- Mucopolysaccharidosis type I
- Multiple sulfatase deficiency
- N-Acetylglutamate synthase deficiency
- Ornithine translocase deficiency
- Otospondylomegaepiphyseal dysplasia
- Persistent Müllerian duct syndrome
- Phenylketonuria
- Reardon-Hall-Slaney syndrome
- Robinow syndrome
- S. Ganesh
- Scheie syndrome
- Spinocerebellar ataxia
- Succinic semialdehyde dehydrogenase deficiency
- Tangier disease
- Tay–Sachs disease
- Thalassemia
- Tyrosinemia
- Tyrosinemia type I
- Urocanic aciduria
- Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Von Willebrand disease
- Wilson's disease
- English Wikipedia @ Freddythechick:Featured picture candidates/pattern of inheritance of autosomal recessive genes
- English Wikipedia @ Freddythechick:Featured pictures/Diagrams, drawings, and maps/Diagrams
- English Wikipedia @ Freddythechick:Featured pictures thumbs/32
- English Wikipedia @ Freddythechick:Main Page history/2014 May 14
- English Wikipedia @ Freddythechick:VideoWiki/Cystic fibrosis
- English Wikipedia @ Freddythechick:WikiProject Medicine/Recognized content
- Template:POTD/2014-05-14