Disease #02684 (OPTA-1 (osteopetrosis, autosomal dominant, type 1 (OPTA-1)), OMIM:607634)

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Official abbreviation	OPTA-1
Name	osteopetrosis, autosomal dominant, type 1 (OPTA-1)
OMIM ID	607634
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LRP5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A