Autosomal dominant chondrodysplasia punctata

MONDO:0007321

Autosomal dominant form of chondrodysplasia punctata.

Also known as: chondrodysplasia punctata Sheffield type, chondrodysplasia punctata, Sheffield type, chondrodysplasia punctata, autosomal dominant, chondrodysplasia punctata due to vitamin K deficiency, chondrodysplasia punctata due to warfarin teratogenicity

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant chondrodysplasia punctata itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7158) ↑ Autosomal dominant disease (699) ↑ Non-rhizomelic chondrodysplasia punctata (1)

Sub-types of Autosomal dominant chondrodysplasia punctata

Chondrodysplasia punctata, brachytelephalangic, autosomal 0 trials
Chondrodysplasia punctata, tibial-metacarpal type 0 trials

Including sub-types (0) Tagged with Autosomal dominant chondrodysplasia punctata (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.