All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01992 OPTB-2 osteopetrosis, autosomal recessive, type 2 (OPTB-2) 259710 - 0 0 TNFSF11 - -
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