About: Haploinsufficiency of A20

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Haploinsufficiency of A20 is a rare disease caused by mutations in the gene TNFAIP3. This gene is also known as A20.

Property	Value
dbo:abstract	Haploinsufficiency of A20 is a rare disease caused by mutations in the gene TNFAIP3. This gene is also known as A20. (en)
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dbp:caption	This condition is inherited in an autosomal dominant manner. (en)
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rdfs:comment	Haploinsufficiency of A20 is a rare disease caused by mutations in the gene TNFAIP3. This gene is also known as A20. (en)
rdfs:label	Haploinsufficiency of A20 (en)
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