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Kidney Tissue Atlas Ontology
Last uploaded:
March 16, 2024
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Preferred Name | inborn disorder of phenylalanin or tyrosine metabolism | |
Synonyms |
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 |
Orphanet:79190 UMLS:CN227599
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exactMatch | ||
has related synonym |
disorder of phenylalanin or tyrosine metabolism
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id |
MONDO:0019235
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imported from | ||
in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
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label |
inborn disorder of phenylalanin or tyrosine metabolism
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|
notation |
MONDO:0019235
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prefLabel |
inborn disorder of phenylalanin or tyrosine metabolism
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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 | EFO | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0019235 | DOVES | SAME_URI |