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inheritance
(redirected from autosomal inheritance)

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inheritance

In biology, the passing of characteristics from parents to offspring. Characteristics that can be passed on in this way are determined by genes (see also allele).

The study of inheritance is called genetics and was founded by the Austrian biologist Gregor Mendel. He found that crossing two parents having one contrasting characteristic (for example, one tall and the other dwarf) showed that inheritance was the consequence of passing on ‘particles’ or, as we now know them, genes, which determine the characteristics. This kind of cross is called a monohybrid cross.

In asexual reproduction the offspring inherit the same characteristics as the parent. In sexual reproduction, the offspring inherit a mix of the characteristics of the two parents.



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Its most common presentation is in the form of sporadic cases, but dominant autosomal inheritance has been described.
 
 
Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Macular Degeneration
Autosomal Dominant Macular Dystrophy
autosomal dominant medullary cystic kidney disease
Autosomal Dominant Motor System Degeneration
Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy
Autosomal Dominant Neurohypophyseal Diabetes Insipidus
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal Dominant Non-Syndromal Hearing Impairment
Autosomal Dominant Non-Syndromic Hearing Loss
Autosomal Dominant Optic Atrophy
Autosomal Dominant Optic Atrophy and Cataract
Autosomal Dominant Partial Epilepsy with Auditory Features
Autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease
Autosomal Dominant Polycystic Liver Disease
Autosomal Dominant Progressive External Ophthalmoplegia
Autosomal Dominant Pure Spastic Paraplegia
Autosomal Dominant Retinitis Pigmentosa
Autosomal Dominant Rolandic Epilepsy with Speech Dyspraxia
Autosomal Dominant Sensory Ataxia
autosomal dominant Stargardt-like disease
Autosomal Dominant Striatal Degeneration
autosomal dominant vitreoretinochoroidopathy
autosomal gene
autosomal inheritance
Autosomal recessive
Autosomal recessive
Autosomal Recessive Charcot-Marie-Tooth
Autosomal Recessive Cone-Rod Dystrophy
autosomal recessive defect
autosomal recessive disease
autosomal recessive disorders
Autosomal Recessive Exfoliative Ichthyosis
autosomal recessive form of rhizomelic chondrodysplasia punctata
autosomal recessive hearing loss
Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hypercholesterolemia
Autosomal recessive inheritance
Autosomal Recessive Juvenile Parkinson's Disease
Autosomal recessive juvenile parkinsonism
Autosomal Recessive Muscular Dystrophy
Autosomal Recessive Muscular Dystrophy of Childhood
Autosomal Recessive Ocular Albinism
Autosomal Recessive Osteopetrosis
Autosomal Recessive Persistent Hyperplastic Primary Vitreous
Autosomal Recessive Polycystic Disease
Autosomal recessive polycystic kidney disease
Autosomal recessive polycystic kidney disease
Autosomal recessive polycystic kidney disease
Autosomal recessive polycystic kidney disease
Autosomal Recessive Sensorineural Hearing Impairment and Goiter
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Autosomal Recessive Vitamin D Dependency
 
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