Bardet-Biedl syndrome 19

MONDO:0014447

Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the IFT27 gene.

Also known as: BBS19, Bardet-Biedl syndrome 19, Bardet-Biedl syndrome caused by mutation in IFT27, Bardet-Biedl syndrome type 19, IFT27 Bardet-Biedl syndrome

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Broader categories

Disease (680) Hereditary disease (176) Syndromic disease (25) Human disease (14) Bardet-Biedl syndrome (6) Autosomal recessive disease (4) Ciliopathy (2) Disease by molecular mechanism (2) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0)

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