Disease #00012 (HP3 (Hyperoxaluria, Primary, Type III), OMIM:613616)

Official abbreviation HP3
Name Hyperoxaluria, Primary, Type III
OMIM ID 613616
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene HOGA1
Associated tissues -
Disease features -
Remarks -


Individuals

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00000057 - M Iran yes - HP3, MPS IVA - GALNS, HOGA1 GALNS, HOGA1 2 1 Variome.ir
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