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Q34896062-186F8550-D3BC-41B3-8B50-FA34E2A85488
Q34896062-186F8550-D3BC-41B3-8B50-FA34E2A85488
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34896062-186F8550-D3BC-41B3-8B50-FA34E2A85488
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement
P2860
Q34896062-186F8550-D3BC-41B3-8B50-FA34E2A85488
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34896062-186F8550-D3BC-41B3-8B50-FA34E2A85488
rank
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type
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Statement
wasDerivedFrom
a418ee9cf70b77c3d9858b5c5a82a59d61cc3bdd
P2860
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis