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Q35885278-47B62AC4-0305-4B9D-8C50-E1C6BBF8A770
Q35885278-47B62AC4-0305-4B9D-8C50-E1C6BBF8A770
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Statement
http://www.wikidata.org/entity/statement/Q35885278-47B62AC4-0305-4B9D-8C50-E1C6BBF8A770
The phenotype of human STK4 deficiency.
P2860
Q35885278-47B62AC4-0305-4B9D-8C50-E1C6BBF8A770
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35885278-47B62AC4-0305-4B9D-8C50-E1C6BBF8A770
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wasDerivedFrom
7215a4287fe2f180e556b8cd52c0d4972b97c714
P2860
Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).