All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05748 HOD hypopigmentation, organomegaly, and delayed myelination and development (HOD) 618541 AD - - CLCN7 - -
05746 OPTA osteopetrosis, autosomal dominant (OPTA) - AD 1 1 CLCN7, LRP5 - -
01483 OPTA2 osteopetrosis, autosomal dominant, type 2 166600 AD 1 1 CLCN7 - -
03033 OPTB4 osteopetrosis, autosomal recessive, type 4 (OPTB4) 611490 AR - - CLCN7 - -
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