A benign, inherited liver disorder characterized by chronic, predominantly conjugated, nonhemolytic hyperbilirubinemia with normal liver histology.
Synonyms: Hyperbilirubinemia, Rotor type
This is just here as a test because I lose it
Term information
database cross reference
- ICD-10:E80.6 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- UMLS:C0220991 (E (Exact mapping: the two concepts are equivalent))
- OMIM:237450 (E (Exact mapping: the two concepts are equivalent))
- MedDRA:10039234 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:E80.6 (Attributed (The ICD10 code is attributed by Orphanet))
Term relations
Subclass of:
- disease
- part_of some Rare metabolic liver disease
- present_in some Worldwide and has_point_prevalence_range some <1 / 1 000 000
- part_of some Disorder of bilirubin metabolism and excretion
- has_inheritance some autosomal recessive
- present_in some Worldwide and has_cases/families_value value 50.0
- has_age_of_onset some all ages