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asphyxiating thoracic dystrophy 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any Jeune syndrome in which the cause of the disease is a mutation in the IFT80 gene.
Uniprot Description A form of short-rib thoracic dysplasia, a group of autosomal recessive ciliopathies that are characterized by a constricted thoracic cage, short ribs, shortened tubular bones, and a 'trident' appearance of the acetabular roof. Polydactyly is variably present. Non-skeletal involvement can include cleft lip/palate as well as anomalies of major organs such as the brain, eye, heart, kidneys, liver, pancreas, intestines, and genitalia. Some forms of the disease are lethal in the neonatal period due to respiratory insufficiency secondary to a severely restricted thoracic cage, whereas others are compatible with life. Disease spectrum encompasses Ellis-van Creveld syndrome, asphyxiating thoracic dystrophy (Jeune syndrome), Mainzer-Saldino syndrome, and short rib-polydactyly syndrome.
Mondo Term and Equivalent IDs
MONDO:0012644:  asphyxiating thoracic dystrophy 2
MESH:C566982: 
UMLS:C1970005: