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Q39031727-F7E21B12-D9A5-4ED6-8590-4BE5C3CCF7FE
Q39031727-F7E21B12-D9A5-4ED6-8590-4BE5C3CCF7FE
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Statement
http://www.wikidata.org/entity/statement/Q39031727-F7E21B12-D9A5-4ED6-8590-4BE5C3CCF7FE
Inherited diseases caused by mutations in cathepsin protease genes.
P2860
Q39031727-F7E21B12-D9A5-4ED6-8590-4BE5C3CCF7FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39031727-F7E21B12-D9A5-4ED6-8590-4BE5C3CCF7FE
rank
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type
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wasDerivedFrom
d855f3a491c99a9bfd9d96f10e231c4c97295003
P2860
Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).