Disease #06360 (OPTA3 (Osteopetrosis, autosomal dominant 3), OMIM:618107)

Official abbreviation OPTA3
Name Osteopetrosis, autosomal dominant 3
OMIM ID 618107
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PLEKHM1
Associated tissues -
Disease features -
Remarks -

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