Disease #00106

Official abbreviation AO-2
Name atelosteogenesis, type II (AO-2, De la Chapelle dysplasia)
OMIM ID 256050
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SLC26A2
Associated tissues -
Disease features -
Remarks -