Disease #01483

Official abbreviation OPTA-2
Name osteopetrosis, autosomal dominant, type 2 (OPTA-2)
OMIM ID 166600
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CLCN7
Associated tissues -
Disease features -
Remarks -