Usher syndrome type 1 Usher syndrome type 1D https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/5438/usher-syndrome-type-1d https://www.malacards.org/card/usher_syndrome_type_id Ush1D/F, Cdh23/Pcdh15, digenic OMIM:601067 USHER syndrome, type ID Usher syndrome, type 1D GARD:0005438 DOID:0110831 Usher syndrome, type 1D/F digenic UMLS:C1832845 USH1D MEDGEN:322051 MONDO:0010984 A form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding cadherin-23 (CDH23) on chromosome 10q22. It is inherited in an autosomal recessive manner. Usher syndrome, type Id/F, Cdh23/Pcdh15, digenic