Disease #03117 (OPTB-7 (osteopetrosis, autosomal recessive, type 7 (OPTB-7)), OMIM:612301)

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Official abbreviation	OPTB-7
Name	osteopetrosis, autosomal recessive, type 7 (OPTB-7)
OMIM ID	612301
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TNFRSF11A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A