Disease #05746 (OPTA (osteopetrosis, autosomal dominant (OPTA)))

Official abbreviation OPTA
Name osteopetrosis, autosomal dominant (OPTA)
OMIM ID -
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes CLCN7, LRP5
Associated tissues -
Disease features -
Remarks -
Date created 2020-05-18 09:27:27 +02:00 (CEST)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
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00387686 FamPatIII.1 PubMed: Gregson 2020 3-generation family, 3 affected (3F) F - United Kingdom (Great Britain) white - - - - OPTA Bone pain (HP:0002653), No Bone fracture (HP:0020110), Myopia (HP:0000545), Mandibular prognathia (HP:0000303), Torus palatinus (HP:0100789) SMAD3, SMAD4, SMAD5, SMAD5-AS1, SMAD6, SMAD7, SMAD9, SMARCAL1 SMAD9 1 3 Litika Vermani
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