Disease #03033 (OPTB4 (osteopetrosis, autosomal recessive, type 4 (OPTB4)), OMIM:611490)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPTB4
Name	osteopetrosis, autosomal recessive, type 4 (OPTB4)
OMIM ID	611490
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLCN7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-18 09:28:57 +02:00 (CEST)

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