File:Autorecessive.svg
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Summary
DescriptionAutorecessive.svg |
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 |
Other versions |
[edit]
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SVG development InfoField | This diagram was created with a text editor. Please do not replace the simplified code of this file with a version created with Inkscape or any other vector graphics editor |
Licensing
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.http://www.gnu.org/copyleft/fdl.htmlGFDLGNU Free Documentation Licensetruetrue |
This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license. | ||
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This licensing tag was added to this file as part of the GFDL licensing update.http://creativecommons.org/licenses/by-sa/3.0/CC BY-SA 3.0Creative Commons Attribution-Share Alike 3.0truetrue |
Annotations InfoField | This image is annotated: View the annotations at Commons |
առողջ կրող հայր
Items portrayed in this file
depicts
25 March 2007
image/svg+xml
08ea22725e02a87e03a0002ead1930d577ba5236
3,491 byte
1,580 pixel
1,350 pixel
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
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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
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- 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 acidemias
- Mitochondrial trifunctional protein deficiency
- Mucolipidosis
- Mucolipidosis type IV
- Mucopolysaccharidosis
- N-Acetylglutamate synthase deficiency
- Omenn syndrome
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- Pendred syndrome
- Persistent Müllerian duct syndrome
- Phenylketonuria
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- Succinic semialdehyde dehydrogenase deficiency
- Sugarman syndrome
- Tangier disease
- Tay–Sachs disease
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- 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.
Metadata
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Width | 1350 |
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Height | 1580 |