autosomal recessive disease · genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop · YYNN

autosomal recessive disease

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genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop

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Subclasses
36

Family of inherited blood disorders

Cystic fibrosis

Genetic disorder inhibiting clearance of mucus from the lungs

Recessive genetic disorder causing deafblindness

Congenital afibrinogenemia

Medical condition

Alström syndrome

Rare genetic disorder involving childhood obesity and multiple organ dysfunction

Bardet–Biedl syndrome

Ciliopathic recessive genetic disorder

Wolfram syndrome 1

Antley–Bixler syndrome

Congenital disorder

Sickle cell disease

Medical condition

Abetalipoproteinemia

Medical condition

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