Disease #02195 (chondrodysplasia, with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, OMIM:300863)

Official abbreviation -
Name chondrodysplasia, with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
OMIM ID 300863
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HDAC6
Associated tissues -
Disease features -
Remarks -