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craniodiaphyseal dysplasia, autosomal dominant

Disease Summary
Associated Targets (1)
Tclin

1


GARD Rare
Uniprot Description A severe bone dysplasia characterized by massive generalized hyperostosis and sclerosis, especially involving the skull and facial bones. The sclerosis is so severe that the resulting facial distortion is referred to as 'leontiasis ossea' (leonine faces) and the bone deposition results in progressive stenosis of craniofacial foramina. Respiratory obstruction due to choanal stenosis compromises the clinical outcomes of affected patients.
Mondo Term and Equivalent IDs
MONDO:0021021:  craniodiaphyseal dysplasia, autosomal dominant
GARD:0000249: 
MESH:C567275: