Disease #01483 (OPTA2 (osteopetrosis, autosomal dominant, type 2), OMIM:166600)

Official abbreviation OPTA2
Name osteopetrosis, autosomal dominant, type 2
OMIM ID 166600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CLCN7
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2025-05-05 09:47:20 +02:00 (CEST)


Individuals

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00359410 Pat8 PubMed: Silveira 2021, Journal: Silveira 2021 - F no Brazil - - - - - OPTA2 see paper; ... - CLCN7 1 1 Maria Dora Jazmin Lacarrubba-Flores
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