File:Autorecessive.svg
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[edit] Summary
| Description |
English: Autosomal recessive gene
Español: Gen autosómica recesiva. Modo de herencia entre dos portadores de un gen autosómica recesiva y monogénica.
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| Date | 25 March 2007 |
| Source | Own work in Inkscape |
| Author | en:User:Cburnett |
| Permission (Reusing this file) |
GFDL |
| Other versions |
Derivative works of this file: File:Autorecessive-es.svg, File:Autorecessive-fr.svg, File:Autorecessive-pl.svg |
By Anesu Venge
[edit] Licensing
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File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 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 link to this file. The following list shows the first 100 page links to this file only. A full list is available.
- Abdallat Davis Farrage syndrome
- Abderhalden–Kaufmann–Lignac syndrome
- Abetalipoproteinemia
- Aceruloplasminemia
- Acheiropodia
- Adducted thumb syndrome
- Adenine phosphoribosyltransferase deficiency
- Adenosine deaminase 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
- Ellis–van Creveld syndrome
- Familial Mediterranean fever
- Familial dysautonomia
- Fanconi anemia
- Fountain syndrome
- Fraser syndrome
- Friedreich's ataxia
- GM2-gangliosidosis, AB variant
- Gastroschisis
- Giant axonal neuropathy
- Gitelman syndrome
- Glutaric acidemia type 2
- Glycogen storage disease type I
- Glycogen storage disease type II
- Glycogen storage disease type III
- Hartnup disease
- Hereditary spastic paraplegia
- Holocarboxylase synthetase deficiency
- Human genetics
- Hurler syndrome
- Impossible syndrome
- Isovaleric acidemia
- Jervell and Lange-Nielsen syndrome
- Lafora disease
- Lamellar ichthyosis
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Lysinuric protein intolerance
- Maple syrup urine disease
- Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Meleda disease
- Metachromatic leukodystrophy
- Methemoglobinemia
- Methylmalonic acidemia
- Mitochondrial trifunctional protein deficiency
- Mucolipidosis
- Mucopolysaccharidosis
- Omenn syndrome
- Otospondylomegaepiphyseal dysplasia
- Pendred syndrome
- Persistent Mullerian duct syndrome
- Phenylketonuria
- Price equation
- Propionic acidemia
- Pseudoxanthoma elasticum
- Recessive
- Sandhoff disease
- Sanfilippo syndrome
- Situs inversus
- Sly syndrome
- Smith-Lemli-Opitz syndrome
- Spinocerebellar ataxia
- Sugarman syndrome
- Tay–Sachs disease
- Tetrahydrobiopterin deficiency
- Thalassemia
- Trimethylaminuria
- Tyrosinemia
- Usher syndrome
- Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Von Willebrand disease
- Waardenburg syndrome
- Walker–Warburg syndrome
- Weissenbacher–Zweymüller syndrome
- Werner syndrome
- Wilson's disease
- Wolman disease
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