File:Autosomal_dominant_-_en.svg
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Summary
DescriptionAutosomal dominant - en.svg |
English: Autosomal dominant - genetics (english version) Français : Transmission autosomique dominante avec un parent porteur (version anglaise) |
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Own work using:
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Français : Domaina |
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Licensing
I, the copyright holder of this work, hereby publish it under the following license:
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Items portrayed in this file
depicts
3 March 2012
image/svg+xml
f3ea28b49e314207e6e4df0d4b427c546b533b53
28,960 byte
1,260 pixel
738 pixel
File history
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 22:33, 5 October 2023 | 738 × 1,260 (31 KB) | Andreyyshore | . | |
21:54, 5 October 2023 | 738 × 1,260 (32 KB) | Andreyyshore | more fixes | ||
21:51, 5 October 2023 | 738 × 1,260 (32 KB) | Andreyyshore | attempting to improve letter spacing for low-resolution rendering | ||
21:40, 5 October 2023 | 738 × 1,260 (31 KB) | Andreyyshore | further fixes | ||
21:35, 5 October 2023 | 738 × 1,260 (31 KB) | Andreyyshore | attempting to fix font size and spacing for newly-added languages | ||
21:29, 5 October 2023 | 738 × 1,260 (31 KB) | Andreyyshore | added Armenian, Romanian, Turkish and Simplified Chinese translations | ||
07:28, 8 August 2021 | 738 × 1,260 (28 KB) | Semso98 | File uploaded using svgtranslate tool (https://svgtranslate.toolforge.org/). Added translation for bs. | ||
12:57, 25 October 2020 | 738 × 1,260 (26 KB) | Kashmiri | Code cleanup and optimisation, typeface replaced with sans-serif | ||
18:27, 21 January 2020 | 738 × 1,283 (75 KB) | SUM1 | Vertically aligned legend boxes | ||
03:44, 21 January 2020 | 738 × 1,283 (75 KB) | SUM1 | Further non-sex-linkage edit |
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.
- Aase syndrome
- Achard syndrome
- Achondrogenesis type 2
- Achondroplasia
- Alagille syndrome
- Albright's hereditary osteodystrophy
- Apolipoprotein B deficiency
- Arakawa's syndrome II
- Autosomal dominant hypophosphatemic rickets
- Axenfeld–Rieger syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- Barakat syndrome
- Birt–Hogg–Dubé syndrome
- Branchio-oto-renal syndrome
- Campomelic dysplasia
- Cardiofaciocutaneous syndrome
- Combined hyperlipidemia
- Costello syndrome
- Darier's disease
- Ectrodactyly–ectodermal dysplasia–cleft syndrome
- Endometrial cancer
- Familial amyloid polyneuropathy
- Familial male-limited precocious puberty
- Flynn–Aird syndrome
- Frontotemporal dementia and parkinsonism linked to chromosome 17
- Gardner's syndrome
- Goldenhar syndrome
- Greig cephalopolysyndactyly syndrome
- Hajdu–Cheney syndrome
- Hemiplegic migraine
- Hereditary hemorrhagic telangiectasia
- Hereditary pancreatitis
- Holt–Oram syndrome
- Human genetics
- Hyperproinsulinemia
- Hypochondroplasia
- Hypokalemic periodic paralysis
- Idiopathic CD4+ lymphocytopenia
- Jackson–Weiss syndrome
- Jansen's metaphyseal chondrodysplasia
- Kniest dysplasia
- Lattice degeneration
- Liddle's syndrome
- Li–Fraumeni syndrome
- Loeys–Dietz syndrome
- Lymphedema–distichiasis syndrome
- Léri–Weill dyschondrosteosis
- MASS syndrome
- Machado–Joseph disease
- Marfan syndrome
- Medullary cystic kidney disease
- Melkersson–Rosenthal syndrome
- Metachondromatosis
- Muckle–Wells syndrome
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2
- Nail–patella syndrome
- Neurofibromatosis
- Noonan syndrome
- Oculopharyngeal muscular dystrophy
- Osteopetrosis
- Pallister–Hall syndrome
- Papillorenal syndrome
- Paramyotonia congenita
- Photic sneeze reflex
- Plantar fibromatosis
- Platyspondylic lethal skeletal dysplasia, Torrance type
- Popliteal pterygium syndrome
- Porphyria cutanea tarda
- Primrose syndrome
- Protein C deficiency
- Reynolds syndrome
- Rubinstein–Taybi syndrome
- SHORT syndrome
- Sack–Barabas syndrome
- Saethre–Chotzen syndrome
- Schmitt Gillenwater Kelly syndrome
- Severe congenital neutropenia
- Sleep
- Sneddon's syndrome
- Spinocerebellar ataxia
- Spinocerebellar ataxia type-13
- Spinocerebellar ataxia type 6
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloperipheral dysplasia
- Sporadic hemiplegic migraine
- Sprengel's deformity
- Stickler syndrome
- TNF receptor associated periodic syndrome
- Tietz syndrome
- Timothy syndrome
- Treacher Collins syndrome
- Tuberous sclerosis
- Uhl anomaly
- Variegate porphyria
- Vitelliform macular dystrophy
- Von Hippel–Lindau disease
- Von Willebrand disease
- Waardenburg syndrome
- Wagner's disease
View more links to this file.
Global file usage
The following other wikis use this file:
- Usage on ar.wikipedia.org
- Usage on az.wikipedia.org
- Usage on bg.wikipedia.org
- Usage on bn.wikipedia.org
- Usage on bs.wikipedia.org
- Forma kose
- Genetika čovjeka
- Naegeli–Franceschetti–Jadassohnov sindrom
- Rubinstein–Taybijev sindrom
- Mišićna distrofija udovi-pojas
- Miotonusna distrofija
- DiGeorgeov sindrom
- Li–Fraumenijev sindrom
- Waardenburgov sindrom
- Albrightova nasljedna osteodistrofija
- Alagilleov sindrom
- Zrelosno ispoljavajući mladalački dijabetes
- Spinocerebelumska ataksija tip 6
- Nasljedna hemoragijska telangiektazija
- Birt–Hogg–Dubéov sindrom
- Miller–Diekerov sindrom
- Kampomelna displazija
- Sindrom mikrodelecije 17q12
- Porfirija cutanea tarda
- Šarena porfirija
- Sindrom duplikacije 1q21.1
- Muckle–Wellsov sindrom
- Sticklerov sindrom
- Sindrom potkoljenskog pterigija
- Jansenova metafizna hondrodisplazija
- Mikrokorija
- Autosomna dominantna očna atrofija
- Von Hippel–Lindauov sindrom
- SADDAN
- Hipohondroplazija
- Eritrokeratodermija varijabilis
- Bosch-Boonstra-Schaafov sindrom optičke atrofije
- Sotosov sindrom
- Razvojna verbalna dispraksija
- Barakatov sindrom
- Osteopetroza
- Usage on cs.wikipedia.org
- Usage on el.wikipedia.org
View more global usage of this file.
Metadata
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If the file has been modified from its original state, some details may not fully reflect the modified file.
Width | 738 |
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Height | 1260 |
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