ochronosis, hereditary

Preferred Label : ochronosis, hereditary;

MeSH synonym : hereditary ochronosis;

Origin ID

C537862;

UMLS CUI

C2931645;

Currated CISMeF NLP mapping
- Alcaptonuria [PASCAL descriptor]
- Alkaptonuria [ORDO Disease]
- Alkaptonuria [OMIM Phenotype]
- Alkaptonuria [MedDRA Preferred Term]
- Homogentisate 1,2-dioxygenase deficiency (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- ochronosis [MeSH Descriptor]
ORDO relation(s)
- Alkaptonuria [ORDO Disease]
Record concept(s)
- Ochronosis, hereditary [MeSH concept]
See also (suggested by CISMeF)
- alkaptonuric ochronosis [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]