Disease #02113 (TYRSN3 (tyrosinemia, type III (TYRSN-3)), OMIM:276710)

Official abbreviation TYRSN3
Name tyrosinemia, type III (TYRSN-3)
OMIM ID 276710
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HPD
Associated tissues -
Disease features -
Remarks -

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