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Experimental Factor Ontology
Last uploaded:
November 18, 2024
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Preferred Name | inborn disorder of phenylalanine and tyrosine metabolism | |
Synonyms |
disorder of phenylalanin or tyrosine metabolism inborn disorder of phenylalanin or tyrosine metabolism |
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ID |
http://purl.obolibrary.org/obo/MONDO_0019235 |
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database_cross_reference |
UMLS:C5681284 MEDGEN:1842953 Orphanet:79190 GARD:18964
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exactMatch |
http://purl.obolibrary.org/obo/Orphanet_79190 |
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has_exact_synonym |
inborn disorder of phenylalanin or tyrosine metabolism
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|
has_related_synonym |
disorder of phenylalanin or tyrosine metabolism
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IAO_0000233 | ||
id |
MONDO:0019235
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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
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|
notation |
MONDO:0019235
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preferred label |
inborn disorder of phenylalanine and tyrosine metabolism
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prefLabel |
inborn disorder of phenylalanine and tyrosine metabolism
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subClassOf | ||
excluded_subClassOf |
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Mapping To | Ontology | Source |
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http://purl.obolibrary.org/obo/MONDO_0019235 | MONDO | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0019235 | OBA | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0019235 | CCONT | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0019235 | DOVES | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0019235 | KTAO | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0019235 | OBA | LOOM |
http://purl.obolibrary.org/obo/MONDO_0019235 | MONDO | LOOM |
http://purl.obolibrary.org/obo/MONDO_0019235 | CCONT | LOOM |
http://purl.obolibrary.org/obo/MONDO_0019235 | DOVES | LOOM |