ochronosis disorder

ochronosis disorder

http://purl.obolibrary.org/obo/MONDO_0001910

A disorder characterized by bluish-black discoloration of the cartilaginous tissues due to accumulation of homogentisic acid. It is associated with alkaptonuria. Signs and symptoms include dark urine, skin pigmentation, and arthritis. [ NCIT:P378 ]

Synonyms: ochronosis

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This is just here as a test because I lose it

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database cross reference

MEDGEN:45177 (MONDO:equivalentTo)
HP:0030764 (MONDO:otherHierarchy)
NCIT:C84938 (MONDO:equivalentTo)
SCTID:410042009 (MONDO:equivalentTo)
DOID:14223 (MONDO:equivalentTo)
UMLS:C0028817 (MONDO:equivalentTo)
ICD9:270.2 (MONDO:relatedTo)
MESH:D009794 (MONDO:equivalentTo)

exactMatch

http://purl.obolibrary.org/obo/DOID_14223

http://purl.obolibrary.org/obo/NCIT_C84938

http://identifiers.org/mesh/D009794

http://linkedlifedata.com/resource/umls/id/C0028817

http://identifiers.org/snomedct/410042009

http://identifiers.org/medgen/45177

MONDO:0001910

Term relations

Equivalent to:

metabolic disease and disease caused by disruption of some homogentisate metabolic process and disease has location some cartilage tissue and disease has feature some Ochronosis

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