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Summary
| Description |
Autosomal dominant - genetics (english version) |
| Date | |
| Source |
Own work using:
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| Author |
Français : Domaina |
| Other versions |
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Licensing
I, the copyright holder of this work, hereby publish it under the following license:
This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license.
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- to remix – to adapt the work
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- attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
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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 | 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.
