Monarch Disease Ontology id MONDO_0800043 (Stüve-Wiedemann syndrome 1) is a rare autosomal recessive congenital primary skeletal dysplasia, characterized by small stature, bowing of the long bones, camptodactyly, hyperthermic episodes, respiratory distress/apneic episodes and feeding difficulties that usually lead to early mortality. Also known as: SJS2, STWS, Schwartz-Jampel syndrome neonatal, Schwartz-Jampel syndrome type 2, Schwartz-Jampel syndrome, neonatal, Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, Stüve-Wiedemann dysplasia, Stüve-Wiedemann/Schwartz-Jampel type 2 syndrome.