" /> Bardet-biedl syndrome 9 - CISMeF





Preferred Label : Bardet-biedl syndrome 9;

Symbol : BBS9;

CISMeF acronym : BBS9;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the parathyroid hormone-responsive B1 gene (PTHB1, 607968.0001);

Prefixed ID : #615986;

Details


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01/11/2024


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