Disease #02684

Official abbreviation OPTA-1
Name osteopetrosis, autosomal dominant, type 1 (OPTA-1)
OMIM ID 607634
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 0
Associated with 1 gene LRP5
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00107589 - - - - - France - - 0 - - OPTA-1 osteopetrosis, autosomal dominant, type 1 LRP5 LRP5 1 2 Johan den Dunnen
00107592 - - - - - Denmark - - 0 - - OPTA-1 osteopetrosis, autosomal dominant, type 1 LRP5 LRP5 1 1 Johan den Dunnen
00107593 - - - - - Denmark - - 0 - - OPTA-1 osteopetrosis, autosomal dominant, type 1 LRP5 LRP5 1 1 Johan den Dunnen
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