File:Autosomal dominant inheritance.jpg: Difference between revisions
mNo edit summary |
mNo edit summary |
||
Line 5: | Line 5: | ||
Autosomal Dominant Disease | Autosomal Dominant Disease | ||
* Huntington’s Disease (HD) - neurodegenerative disorder characterised by progressive motor abnormality and cognitive deterioration. (More? [[2011_Group_Project_4|Student Project]]) | * Huntington’s Disease (HD) - neurodegenerative disorder characterised by progressive motor abnormality and cognitive deterioration. (More? [[2011_Group_Project_4|Student Project]]) | ||
* Autosomal Dominant Polycystic Kidney Disease (ADPKD) - late-onset multisystem disorder characterized by bilateral renal cysts, liver cysts, and an increased risk of intracranial aneurysms. (heterozygous pathogenic variant in PKD1, PKD2, GANAB, or DNAJB11) | |||
{{GHR Inheritance}} | {{GHR Inheritance}} | ||
'''Links:''' | '''Links:''' {{spermatozoa}} | {{oocyte}} | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=autosomal_inheritance Search Pubmed - autosomal inheritance] | ||
Line 21: | Line 24: | ||
Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html | Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html | ||
{{Footer}} | |||
[[Category:Genetics]] [[Category:Meiosis]] | [[Category:Genetics]] [[Category:Meiosis]] |
Revision as of 10:51, 23 July 2018
Autosomal dominant inheritance
In this example, a man with an autosomal dominant disorder has two affected children and two unaffected children.
Autosomal Dominant Disease
- Huntington’s Disease (HD) - neurodegenerative disorder characterised by progressive motor abnormality and cognitive deterioration. (More? Student Project)
- Autosomal Dominant Polycystic Kidney Disease (ADPKD) - late-onset multisystem disorder characterized by bilateral renal cysts, liver cysts, and an increased risk of intracranial aneurysms. (heterozygous pathogenic variant in PKD1, PKD2, GANAB, or DNAJB11)
- Inheritance Pattern images: Genetic Abnormalities | autosomal dominant | autosomal recessive | X-linked dominant (affected father) | X-Linked dominant (affected mother) | X-Linked recessive (affected father) | X-Linked recessive (carrier mother) | mitochondrial inheritance | Codominant inheritance | Genogram symbols | Genetics
Links: spermatozoa | oocyte | Search Pubmed - autosomal inheritance
Reference
Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autodominant
Copyright
Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html
Cite this page: Hill, M.A. (2024, April 18) Embryology Autosomal dominant inheritance.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Autosomal_dominant_inheritance.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 09:40, 12 May 2010 | 307 × 396 (64 KB) | S8600021 (talk | contribs) | Autosomal dominant inheritance In this example, a man with an autosomal dominant disorder has two affected children and two unaffected children. Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autodominant Government info |
You cannot overwrite this file.
File usage
The following 15 pages use this file:
- 2010 BGD Practical 3 - Gametogenesis
- 2011 Lab 1 - Gametogenesis
- A
- ANAT2341 Lab 1 - Gametogenesis
- ANAT2341 Lab 3 2013
- Abnormal Development - Genetic
- BGDA Practical 3 - Gametogenesis
- Fetal Cells in Maternal Blood
- Genome Sequencing
- K12 Professional Development 2014
- Molecular Development - Genetics
- Non-Invasive Prenatal Testing
- Preimplantation Genetic Diagnosis
- Prenatal Diagnosis
- User:Z5001524