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spondylocostal dysostosis 3, autosomal recessive

Disease Summary
Associated Targets (5)
Tbio

5


GARD Rare
Mondo Description Any autosomal recessive spondylocostal dysostosis in which the cause of the disease is a mutation in the LFNG gene.
Uniprot Description A condition of variable severity associated with vertebral and rib segmentation defects. The main skeletal malformations include fusion of vertebrae, hemivertebrae, fusion of certain ribs, and other rib malformations. Deformity of the chest and spine (severe scoliosis, kyphoscoliosis and lordosis) is a natural consequence of the malformation and leads to a dwarf-like appearance. As the thorax is small, infants frequently have respiratory insufficiency and repeated respiratory infections resulting in life-threatening complications in the first year of life.
Mondo Term and Equivalent IDs
MONDO:0012349:  spondylocostal dysostosis 3, autosomal recessive
GARD:0004973: 
UMLS:C1853296: