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X-linked chondrodysplasia punctata 1

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Brachytelephalangic chondrodysplasia punctata (BCDP) is a form of nonrhizomelic chondrodysplasia punctata, a primary bone dysplasia, characterized by hypoplasia of the distal phalanges of the fingers, nasal hypoplasia, epiphyseal stippling appearing in the first year of life, and mild and nonrhizomelic shortness of the long bones.
Uniprot Description A clinically and genetically heterogeneous disorder characterized by punctiform calcification of the bones. CDPX1 is a congenital defect of bone and cartilage development characterized by aberrant bone mineralization, severe underdevelopment of nasal cartilage, and distal phalangeal hypoplasia. This disease can also be induced by inhibition with the drug warfarin.
Mondo Term and Equivalent IDs
MONDO:0010555:  X-linked chondrodysplasia punctata 1
GARD:0001296: 
Orphanet:79345: 
UMLS:C1844853: 
UMLS:C3669395: