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bn:14512446n

Noun Concept

EN

autosomal recessive disease autosomal recessive hereditary disease autosomal recessive hereditary disorder autosomal recessive inherited disease autosomal recessive inherited disorder

EN

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 Wikidata

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EN

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 Wikidata

IS A

HAS KIND

abetalipoproteinemia

cystic fibrosis

congenital afibrinogenemia

sickle-cell anemia

HAS INSTANCE

trimethylaminuria

HAS CAUSE

MODE OF INHERITANCE

Wikidata

EN

autosomal recessive disease

Wikidata Alias

EN

autosomal recessive hereditary disease, autosomal recessive hereditary disorder, autosomal recessive inherited disease, autosomal recessive inherited disorder, disease, autosomal recessive, recessive hereditary disorder (autosomal)