NIH GARD Information: Rhizomelic chondrodysplasia punctata type 2
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- Dihydroxyacetonephosphate acyltransferase deficiency
- DHAPAT deficiency
- Peroxisomal dihydroxyacetonephosphate acyltransferase deficiency
- Type 2 rhizomelic chondrodysplasia punctata
- Chondrodysplasia punctata, rhizomelic, due to dihydroxyacetonephosphate
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.