Bardet-Biedl syndrome 18

MONDO:0014446

Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the BBIP1 gene.

Also known as: BBIP1 Bardet-Biedl syndrome, BBS18, Bardet-Biedl syndrome 18, Bardet-Biedl syndrome caused by mutation in BBIP1, Bardet-Biedl syndrome type 18

0 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

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)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.