A form of Jeune syndrome caused by biallelic loss-of-function variants in the GRK2 gene. The disease is MONDO_0100583 (Jeune syndrome - GRK2-related). Also known as: GRK2-related Jeune syndrome, asphyxiating thoracic dystrophy - GRK2-related, short rib polydactyly - GRK2 related, short rib thoracic dystrophy - GRK2 related.