chondrodysplasia calcificans congenita

chon·dro·dys·pla·si·a cal·ci·f'i·cans con·gen·'i·ta

[MIM*118650] autosomal dominant inheritance characterized by asymmetric calcifications and dysplastic skeletal changes, less frequent occurrence of congenital cataracts and ichthyosis compared with other forms, and relatively good prognosis. Synonym(s): Conradi disease, Conradi-Hünermann disease

chon·dro·dys·pla·si·a cal·ci·fi·cans con·gen·i·ta

(kon'drō-dis-plā'zē-ă kal-sif'i-kanz kon-jen'i-tă) A form of hereditary chondrodysplasia characterized by asymmetric calcifications, dysplastic skeletal changes, and relatively good prognosis.
Synonym(s): Conradi disease.