Dubin-Johnson syndrome
rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum
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Dubin-Johnson syndrome
Summary
Dubin-Johnson syndrome is a rare disease[1]. It draws 229 Wikipedia views per month (rare_disease category, ranking #165 of 627).[2]
Key Facts
- Dubin-Johnson syndrome's instance of is recorded as rare disease[3].
- Dubin-Johnson syndrome's instance of is recorded as class of disease[4].
- Dubin-Johnson syndrome is a type of bilirubin metabolic disorder[5].
- Dubin-Johnson syndrome is a type of rare metabolic liver disease[6].
- Dubin-Johnson syndrome is a type of disease[7].
- Dubin-Johnson syndrome's NCI Thesaurus ID is recorded as C34741[8].
- Dubin-Johnson syndrome's health specialty is recorded as pediatrics[9].
- Dubin-Johnson syndrome's health specialty is recorded as hepatology[10].
- Dubin-Johnson syndrome's genetic association is recorded as ABCC2[11].
- Dubin-Johnson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12308[12].
- Dubin-Johnson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:12308[13].
- Dubin-Johnson syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_234[14].
- Dubin-Johnson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Dubin-Johnson syndrome draws 229 Wikipedia views per month (rare_disease category, ranking #165 of 627).[2] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[16] It is known by 19 alternative names across languages and contexts.[17]