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

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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	-
Phenotype entries for this disease	-
Associated with 1 gene	TNFSF11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A