(Q55788556)

English

inborn disorder of phenylalanine or tyrosine metabolism

human disease

Disorder of phenylalanine or tyrosine metabolism
Abnormality of phenylalanine or tyrosine metabolism

In more languages

Statements

class of disease

0 references

amino acid metabolic disorder

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http://www.orpha.net/ORDO/Orphanet_79190

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Identifiers

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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