Hyperbilirubinemia, conjugated, type III

Preferred Label : Hyperbilirubinemia, conjugated, type III;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 237550;

Details

Origin ID

237550;

UMLS CUI

C0400964;

Currated CISMeF NLP mapping
- Hyperbilirubinemia - conjugated - type III (disorder) [SNOMED CT concept]
- hyperbilirubinemia, conjugated, type III [MeSH concept]
- hyperbilirubinemia, conjugated, type III [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Conjugated hyperbilirubinemia [HPO term]
- Jaundice [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperbilirubinemia - conjugated - type III (disorder) [SNOMED CT concept]
- hyperbilirubinemia, conjugated, type III [MeSH Supplementary Concept]
- hyperbilirubinemia, conjugated, type III [MeSH concept]

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