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Summary
| Description |
English: Autosomal recessive gene Español: Gen autosómico recesivo. Modo de herencia entre dos portadores de un gen autosómico recesivo y monogénico. |
| Date | |
| Source | Own work in Inkscape |
| Author | en:User:Cburnett |
| Permission (Reusing this file) |
GFDL |
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Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the section entitled GNU Free Documentation License. |
  
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| Annotations | This image is annotated: View the annotations at Commons |
File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 18:06, 18 September 2023 | | 1,350 × 1,580 (3 KB) | Puck04 | remake (by hand); path text --> <text> |
| 01:14, 27 October 2019 |  | 1,350 × 1,580 (75 KB) | Reywas92 | Rm unnecessary scare quotes | |
| 18:01, 21 April 2007 |  | 1,350 × 1,580 (38 KB) | Cburnett | Enlarge "R" and "r" circles; combined caption of unaffected carriers into one. | |
| 12:51, 21 April 2007 |  | 1,350 × 1,580 (38 KB) | Lwollert | {{Information |Description={{en|Autosomal recessive gene inheritance}} |Source=en:User:Cburnett's work in Inkscape, minor alteration in inkscape |Date=April 21, 2007 |Author=en:User:Cburnett |Permission=G | |
| 19:26, 25 March 2007 |  | 1,350 × 1,580 (38 KB) | Cburnett | Fix arrows | |
| 19:18, 25 March 2007 |  | 1,350 × 1,580 (36 KB) | Cburnett | {{Information |Description={{en|Autosomal recessive gene}} |Source=Own work in Inkscape |Date=March 25, 2007 |Author=en:User:Cburnett |Permission=GFDL |other_versions= }} |
File usage
More than 100 pages use this file. The following list shows the first 100 pages that use this file only. A full list is available.
- 2-Hydroxyglutaric aciduria
- Abetalipoproteinemia
- Aceruloplasminemia
- Acheiropodia
- Acrodermatitis enteropathica
- Adducted thumb syndrome
- Adenine phosphoribosyltransferase deficiency
- Adenylosuccinate lyase deficiency
- Alpha-mannosidosis
- Apparent mineralocorticoid excess syndrome
- Ataxia–telangiectasia
- Atelosteogenesis, type II
- Batten disease
- Behr syndrome
- Berdon syndrome
- Beta-ketothiolase deficiency
- Biotinidase deficiency
- Bloom syndrome
- Blue diaper syndrome
- Canavan disease
- Carnitine-acylcarnitine translocase deficiency
- Carnitine palmitoyltransferase II deficiency
- Carnitine palmitoyltransferase I deficiency
- Carpenter syndrome
- Cartilage–hair hypoplasia
- Chondrodystrophy
- Cockayne syndrome
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Craniodiaphyseal dysplasia
- Cystic fibrosis
- Cystinosis
- Diastrophic dysplasia
- Dubin–Johnson syndrome
- Familial Mediterranean fever
- Familial dysautonomia
- Fanconi anemia
- Fountain syndrome
- Fraser syndrome
- Friedreich's ataxia
- Fumarase deficiency
- GM2-gangliosidosis, AB variant
- Giant axonal neuropathy
- Gitelman syndrome
- Glutaric acidemia type 2
- Glycine encephalopathy
- Glycogen storage disease type I
- Glycogen storage disease type II
- Glycogen storage disease type III
- Griscelli syndrome
- Hartnup disease
- Histidinemia
- Holocarboxylase synthetase deficiency
- Human genetics
- Hurler syndrome
- Isovaleric acidemia
- Jervell and Lange-Nielsen syndrome
- Lafora disease
- Leukodystrophy
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Lucey–Driscoll syndrome
- Lysinuric protein intolerance
- Meleda disease
- Methemoglobinemia
- Methylmalonic acidemia
- Mitochondrial trifunctional protein deficiency
- Mucolipidosis
- Mucolipidosis type IV
- Mucopolysaccharidosis
- N-Acetylglutamate synthase deficiency
- Omenn syndrome
- Otospondylomegaepiphyseal dysplasia
- Pendred syndrome
- Persistent Müllerian duct syndrome
- Phenylketonuria
- Progressive familial intrahepatic cholestasis
- Propionic acidemia
- Pseudoxanthoma elasticum
- Robinow syndrome
- Situs inversus
- Sly syndrome
- Spinocerebellar ataxia
- Succinic semialdehyde dehydrogenase deficiency
- Sugarman syndrome
- Tangier disease
- Tay–Sachs disease
- Tetrahydrobiopterin deficiency
- Thalassemia
- Trimethylaminuria
- Tyrosinemia
- Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Von Willebrand disease
- Walker–Warburg syndrome
- Weissenbacher–Zweymüller syndrome
- Werner syndrome
- Wilson's disease
- Wolfram syndrome
- Xeroderma pigmentosum
- ZAP70 deficiency
- Talk:Dominance (genetics)
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Global file usage
The following other wikis use this file:
- Usage on ar.wikipedia.org
- Usage on bg.wikipedia.org
- Usage on bn.wikipedia.org
- Usage on bs.wikipedia.org
- Genetika čovjeka
- Perzistentni sindrom Müllerovog kanala
- Metahromatska leukodistrofija
- Methemoglobinemija
- Nedostatak holokarboksilazne sintetaze
- Jervellov i Lange-Nielsenov sindrom
- Sindrom arterijske vijugavosti
- Donohueov sindrom
- Bolest s mokraćom mirisa javorovog sirupa
- Cistična fibroza
- Cistinoza
- Bolest skladištenja glikogena tipa II
- Canavanova bolest
- Mukopolisaharidoza
- Nedostatak acil-koenzima dugolančane A dehidrogenaze
- Battenova bolest
- Porodična mediteranska groznica
- Talasemija
- Tirozinemija
- Ravna rožnjača
- Trimetilaminurija
- Nedostatak karnitin-palmitoiltransferaze II
- Tay-Sachsova bolest
- Bloomov sindrom
- Nedostatak 3-hidroksiacil-koenzima dugolančane dehidrogenaze A
- Nedostatak mitohondrijskog trifunkcionalnog proteina
- Atransferinemija
- Nedostatak biotinidaze
- Nedostatak karnitin-acilkarnitin translokaze
- Seckelov sindrom
- Propionska acidemija
- Xeroderma pigmentosum
- Wolframov sindrom
- Muenkeov sindrom
- Metilmalonska acidemija
- Nedostatak tetrahidrobiopterina
- Ahondrogeneza tip 1B
- Atelosteogeneza tip II
- AB varijanta GM2-gangliozidoze
- Cockayneov sindrom
- Diastrofijska displazija
- Sandhoffova bolest
- Nethertonov sindrom
- Epifizna multipla recesivna displazija
- Nedostatak 21-hidroksilaze
View more global usage of this file.
