Disease #03117 (OPTB7 (osteopetrosis, autosomal recessive, type 7 (OPTB-7)), OMIM:612301)

Official abbreviation OPTB7
Name osteopetrosis, autosomal recessive, type 7 (OPTB-7)
OMIM ID 612301
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene TNFRSF11A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00359411 Pat55 PubMed: Silveira 2021, Journal: Silveira 2021 - F ? Brazil - - - - - OPTB7 - - TNFRSF11A 1 1 Maria Dora Jazmin Lacarrubba-Flores
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