Disease #01992 (OPTB-2 (osteopetrosis, autosomal recessive, type 2 (OPTB-2)), OMIM:259710)

Official abbreviation OPTB-2
Name osteopetrosis, autosomal recessive, type 2 (OPTB-2)
OMIM ID 259710
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TNFSF11
Associated tissues -
Disease features -
Remarks -