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

Official abbreviation OPTB-7
Name osteopetrosis, autosomal recessive, type 7 (OPTB-7)
OMIM ID 612301
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene TNFRSF11A
Associated tissues -
Disease features -
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Individuals

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00359411 03149 - - F ? Brazil - - 0 - - OPTB-7 - - - 0 1 Maria Dora Jazmin Lacarrubba-Flores
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