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inborn disorder of histidine metabolism

Go to external page http://purl.obolibrary.org/obo/MONDO_0019228

An inherited metabolic disease that is has its basis in the disruption of histidine metabolic process. [ MONDO:patterns/inborn_metabolic ]

Synonyms: inborn disorder of histidine metabolism histidine metabolic process disease disorder of histidine metabolic process histidine metabolism disease disorder of histidine metabolism rare inborn error of histidine metabolic process inborn error of histidine metabolic process inborn error of histidine metabolism inborn histidine metabolic process disorder disturbance of histidine metabolism

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:18959 (Orphanet:79181)
  • Orphanet:79181 (MONDO:equivalentTo)
  • SCTID:44176004 (MONDO:equivalentTo)
  • DOID:9265 (MONDO:equivalentTo)
  • ICD10CM:E70.40 (MONDO:equivalentTo)
  • ICD9:270.5 (DOID:9265)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

IAO 0000233

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

https://github.com/monarch-initiative/mondo/issues/5364

exactMatch

http://identifiers.org/snomedct/44176004

http://www.orpha.net/ORDO/Orphanet_79181

http://purl.bioontology.org/ontology/ICD10CM/E70.40

http://purl.obolibrary.org/obo/DOID_9265

excluded subClassOf

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

id

MONDO:0019228