Conradi-Hünermann Syndrome

Chondrodysplasia Punctata 2, X-Linked Dominant
Source/Author: OMIM, Online Mendelian Inheritance in Man 
Web-based (medical)
Medical/Scientific description of Chondrodysplasia Punctata, type 2 with emphasis on the genetics of the condition. Conradi-Hünermann Syndrome is the same condition as X-linked dominant Chondrodysplasia Punctata.

Conradi Hünermann Syndrome
Source/Author: National Organization for Rare Disorders (NORD)
Web-based (medical)
Description of the clinical features/characteristics, medical complications and genetics of this condition.

Medical Information - Conradi-Hünermann Syndrome
Source/Author: Restricted Growth Association 
Web-based (lay)
Basic overview of this condition. 

X-linked Dominant Chondrodysplasia Punctata
Source/Author: Neil V Whittock and Louise Izatt; Orphanet 
Web-based (medical)
Detailed overview of this condition. Conradi-Hünermann Syndrome is the same condition as X-linked dominant Chondrodysplasia Punctata.