Renal ciliopathiesGene: WDPCP
Confirmed association with Bardet-Biedl Syndrome type 15 in Gene2Phenotype.
Created: 20 Jul 2018, 1:42 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Comment on list classification: Single patient in OMIM
Created: 17 Dec 2015, 3:01 p.m.
gene: WDPCP was added gene: WDPCP was added to Renal ciliopathies. Sources: Emory Genetics Laboratory,Expert list,UKGTN,Radboud University Medical Center, Nijmegen,Orphanet,Expert Review Green Mode of inheritance for gene: WDPCP was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: WDPCP were set to 20671153 Phenotypes for gene: WDPCP were set to ?Bardet-Biedl syndrome 15, 615992; Meckel syndrome; ?Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085