- Institution/s: Rheinische Friedrich-Wilhelms-Universität Bonn, Universidad de Valladolid
- Project: Diccionario Terminológico de Genética (Eurogene)
- Identification number: 63
- Subdomains: Studies of chromatin, Studies of DNA, Studies of RNA, Techniques
- Author/s: Ana María ALCONCHEL SEBASTIÁN, Beatriz BURGOS CUADRILLERO, Inés PLAZA FONTANET, Patricia ROJO DE DOMINGO
- Creation / modification date: 30-01-2014
- Term: autosomal dominant inheritance
- Gramatical category: s
- Definition: Transmission of a gene with is located on one of the autosomes and one copy is sufficient for the trait to be expressed and or for the disease to be present.
- Context: Although transmission of a disease through members of either sex through multiple generations of a family strongly suggests autosomal dominant inheritance, it is important to remember that autosomal dominant diseases can occur without a positive family history.
- Notes: In autosomal dominant inheritance penetrance may be incomplete, so the gene may appear to “skip” a generation.
- Weighting mark: nor
- Remission: sin, autosomal anomaly(ies) . Source: JEQUIER, A M. (2000). Male infertility. Oxford: Blackwell Science Ltd.
- Sources:
- Term: EMERY, A.E.H. y MUELLER, R.F. (1992) Elements of Medical Genetics, Churchill Livingstone: New York. 8th Edition.
- Definition: HABERMAN T. M., & GHOSH Amit K. (Eds.) (2008). Mayo Clicic Internal Medicine. Rochester: Mayo Foundation for Medical Education and Research
- Context: HABERMAN T. M., & GHOSH Amit K. (Eds.) (2008). Mayo Clicic Internal Medicine. Rochester: Mayo Foundation for Medical Education and Research
- Notes: TUCKER BLACKBURN, S. (2007). Maternal, fetal, & neonatal physiology: clinical perspective. St. Louis: Saunders Elsevier
- Images:
Genagen: Herencia autosómica dominante. Recuperado el 28 de abril de 2013 desde http://www.genagen.es/area-pacientes/informacion-sobre-enfermedades-hereditarias/item/herencia-autosomica-dominante.html
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