All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01483 OPTA-2 osteopetrosis, autosomal dominant, type 2 (OPTA-2) 166600 - 0 0 CLCN7 - -
03033 OPTB-4 osteopetrosis, autosomal recessive, type 4 (OPTB-4) 611490 - 0 0 CLCN7 - -
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