Disease #02684 (OPTA1 (osteopetrosis, autosomal dominant, type 1), OMIM:607634)

Official abbreviation OPTA1
Name osteopetrosis, autosomal dominant, type 1
OMIM ID 607634
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene LRP5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2025-05-05 09:47:03 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00107589 FamG PubMed: Van Wesenbeeck 2003 - - - France - - - - - OPTA1 osteopetrosis, autosomal dominant, type 1 LRP5 LRP5 1 2 Johan den Dunnen
00107592 FamI PubMed: Van Wesenbeeck 2003 - - - Denmark - - - - - OPTA1 osteopetrosis, autosomal dominant, type 1 LRP5 LRP5 1 1 Johan den Dunnen
00107593 FamJ PubMed: Van Wesenbeeck 2003 - - - Denmark - - - - - OPTA1 osteopetrosis, autosomal dominant, type 1 LRP5 LRP5 1 1 Johan den Dunnen
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