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Q28081939-DBF3E2A9-57DB-4432-97E0-CFFB2AABD521
Q28081939-DBF3E2A9-57DB-4432-97E0-CFFB2AABD521
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Statement
http://www.wikidata.org/entity/statement/Q28081939-DBF3E2A9-57DB-4432-97E0-CFFB2AABD521
Nephronophthisis and related syndromes
P2860
Q28081939-DBF3E2A9-57DB-4432-97E0-CFFB2AABD521
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28081939-DBF3E2A9-57DB-4432-97E0-CFFB2AABD521
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Statement
wasDerivedFrom
7d9974667f764e239022bc4c95581f7e1cec5492
P2860
Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis