BH4-deficient hyperphenylalaninemia A
human disease
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BH4-deficient hyperphenylalaninemia A
Summary
BH4-deficient hyperphenylalaninemia An is a genetic disease[1]. It draws 150 Wikipedia views per month (genetic_disease category, ranking #13 of 16).[2]
Key Facts
- BH4-deficient hyperphenylalaninemia A's instance of is recorded as genetic disease[3].
- BH4-deficient hyperphenylalaninemia A's instance of is recorded as rare disease[4].
- BH4-deficient hyperphenylalaninemia A's instance of is recorded as class of disease[5].
- BH4-deficient hyperphenylalaninemia An is a type of hyperphenylalaninemia[6].
- BH4-deficient hyperphenylalaninemia An is a type of amino acid metabolic disorder[7].
- BH4-deficient hyperphenylalaninemia An is a type of enzymopathy[8].
- BH4-deficient hyperphenylalaninemia A's NCI Thesaurus ID is recorded as C138171[9].
- BH4-deficient hyperphenylalaninemia A's genetic association is recorded as PTS[10].
- BH4-deficient hyperphenylalaninemia A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090106[11].
- BH4-deficient hyperphenylalaninemia A's exact match is recorded as http://identifiers.org/doid/DOID:0090106[12].
- BH4-deficient hyperphenylalaninemia A's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_13[13].
- BH4-deficient hyperphenylalaninemia A's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
BH4-deficient hyperphenylalaninemia A draws 150 Wikipedia views per month (genetic_disease category, ranking #13 of 16).[2] It is known by 10 alternative names across languages and contexts.[15]