Disease #01833 (HPABH4B (Hyperphenylalaninemia, BH4-deficient, B), OMIM:233910)

Official abbreviation HPABH4B
Name Hyperphenylalaninemia, BH4-deficient, B
OMIM ID 233910
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 GCH1
Associated tissues -
Disease features -
Remarks -

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