Disease #04478 (BRKS1 (Bruck syndrome, type 1 (BRKS1)), OMIM:259450)

Official abbreviation BRKS1
Name Bruck syndrome, type 1 (BRKS1)
OMIM ID 259450
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FKBP10
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.