Experimental Factor Ontology

Last uploaded: June 18, 2024
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Preferred Name

inborn disorder of phenylalanine and tyrosine metabolism
Synonyms

inborn disorder of phenylalanin or tyrosine metabolism

disorder of phenylalanin or tyrosine metabolism
ID

http://purl.obolibrary.org/obo/MONDO_0019235
database_cross_reference

Orphanet:79190

GARD:18964
exactMatch

http://purl.obolibrary.org/obo/Orphanet_79190
has_exact_synonym

inborn disorder of phenylalanin or tyrosine metabolism
has_related_synonym

disorder of phenylalanin or tyrosine metabolism
IAO_0000233

https://github.com/monarch-initiative/mondo/issues/4985
id

MONDO:0019235
in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders

http://purl.obolibrary.org/obo/mondo/mondo-base#disease_grouping
label

inborn disorder of phenylalanine and tyrosine metabolism
notation

MONDO:0019235
prefLabel

inborn disorder of phenylalanine and tyrosine metabolism
subClassOf

http://purl.obolibrary.org/obo/MONDO_0004736
excluded_subClassOf

http://purl.obolibrary.org/obo/MONDO_0019189
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