Examples of 'is an autosomal recessive' in a sentence
Meaning of "is an autosomal recessive"
is an autosomal recessive: Indicates a genetic trait or disorder that is inherited due to a recessive gene on an autosome, a non-sex chromosome
How to use "is an autosomal recessive" in a sentence
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is an autosomal recessive
This is an autosomal recessive inborn error of metabolism.
This causes insulin resistance and is an autosomal recessive disorder.
Omenn syndrome is an autosomal recessive severe combined immunodeficiency.
Hypotrichosis with juvenile macular dystrophy is an autosomal recessive hereditary disease.
It is an autosomal recessive disorder that is sometimes seen in siblings.
Toulouse Lautrec Syndrome is an autosomal recessive disease.
It is an autosomal recessive congenital disease.
Sickle-cell anemia is an autosomal recessive disease.
It is an autosomal recessive disease, which means that both parents must be carriers.
Lastly, congenital hepatic fibrosis is an autosomal recessive malformation.
There is an autosomal recessive gene dr which affects remigesand rectrices.
For these reasons, it is believed that PCD is an autosomal recessive genetic alteration.
Trimethylaminuria is an autosomal recessive disorder involving a trimethylamine oxidase deficiency.
Oculocutaneous albinism type I or type 1A is an autosomal recessive skin disease.
Galactosemia is an autosomal recessive inherited disorder detectable in newborns and childhood.
See also
Introduction, gaucher disease ( gd ) is an autosomal recessive genetic disease.
Ichthyosis is an autosomal recessive disorder associated with cuneiform cataracts and nuclear sclerosis.
Gaucher disease is an autosomal recessive disorder.
CIE is an autosomal recessive genetic disorder.
Cystic fibrosis CF is an autosomal recessive genetic disease.
IS is an autosomal recessive condition.
The receptor defect is an autosomal recessive mutation or polymorphism.
CF is an autosomal recessive disease.
Nevo Syndrome is an autosomal recessive disorder.
It is an autosomal recessive cerebellar ataxia ( ARCA ) associated with hypoalbuminemia and hypercholesterolemia.
Xeroderma pigmentosum ( xp ) variant is an autosomal recessive disease that involves changes in polh.
SIOD is an autosomal recessive disorder.
GM1 gangliosidosis is an autosomal recessive disease.
Cystic Fibrosis is an autosomal recessive hereditary disease that affects cells of various organs.
Hoof wall separation disease, ( HWSD ), is an autosomal recessive genetic hoof disease in horses.
This is an autosomal recessive inherited disorder, which means that,.
Cerebellar Ataxia is an autosomal recessive neurological disease.
Genetically, it is an autosomal recessive disorder, making its occurrence fairly rare.
Hypomagnesemia with secondary hypocalcemia ( HSH ) is an autosomal recessive genetic disorder affecting intestinal magnesium absorption.
Gaucher 's disease is an autosomal recessive genetic disease caused by a deficiency of a lysosomal enzyme, beta-glucocerebrosidase.
Mucolipidosis type IV ( ML IV ) is an autosomal recessive lysosomal storage disorder.
Since HPS is an autosomal recessive disorder, both parents are carriers of the abnormal gene.
Sjögren-Larsson syndrome (SLS) is an autosomal recessive form of ichthyosis apparent at birth.
This disorder is an autosomal recessive form of xanthomatosis.
Cystic fibrosis CF is an autosomal recessive disease that is irreversible.
Cystic fibrosis CF is an autosomal recessive disease that is highly prevalent among caucasians.
Hereditary hemochromatosis is an autosomal recessive disease and generally due to mutations in HFE gene.
Wilson 's disease is an autosomal recessive disorder of copper metabolism.
Sickle cell disease ( scd ) is an autosomal recessive disease characterized by a mutation in hemoglobin.
Nephropathic cystinosis ( nc ) is an autosomal recessive systemic severe disease characterized by intralysosomal cystine accumulation.
Wolfram 's syndrome is an autosomal recessive neurodegenerative disorder that first becomes evident in childhood.
Urocanic aciduria, is an autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase.
Alpha-mannosidosis is an autosomal recessive metabolic disorder that causes mental and physical deterioration.
Cystic fibrosis ( CF ) is an autosomal recessive genetic disease causing inborn error of metabolism.
Cystic fibrosis CF is an autosomal recessive genetic disease of chronic, progressive, and irreversible evolution.
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Examples of using Recessive
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Two points about recessive mutations are important
Recessive according to their intensity and effect
This is an autosomal recessive inborn error of metabolism
Examples of using Autosomal
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This is an autosomal recessive inborn error of metabolism
The condition is inherited in an autosomal recessive pattern
Autosomal dominant nocturnal frontal lobe epilepsy
