arthrogryposis–renal dysfunction–cholestasis syndrome
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Summary
arthrogryposis–renal dysfunction–cholestasis syndrome is a rare disease[1]. It draws 14 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]
Key Facts
- arthrogryposis–renal dysfunction–cholestasis syndrome's instance of is recorded as rare disease[3].
- arthrogryposis–renal dysfunction–cholestasis syndrome's instance of is recorded as class of disease[4].
- arthrogryposis–renal dysfunction–cholestasis syndrome is a type of neurogenic arthrogryposis multiplex congenita[5].
- arthrogryposis–renal dysfunction–cholestasis syndrome is a type of tubulopathy[6].
- arthrogryposis–renal dysfunction–cholestasis syndrome is a type of cholestasis[7].
- arthrogryposis–renal dysfunction–cholestasis syndrome is a type of syndrome[8].
- arthrogryposis–renal dysfunction–cholestasis syndrome is a type of autosomal recessive disease[9].
- arthrogryposis–renal dysfunction–cholestasis syndrome's health specialty is recorded as dermatology[10].
- arthrogryposis–renal dysfunction–cholestasis syndrome's genetic association is recorded as VPS33B[11].
- arthrogryposis–renal dysfunction–cholestasis syndrome's genetic association is recorded as VIPAS39[12].
- arthrogryposis–renal dysfunction–cholestasis syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050763[13].
- arthrogryposis–renal dysfunction–cholestasis syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050763[14].
- arthrogryposis–renal dysfunction–cholestasis syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2697[15].
- arthrogryposis–renal dysfunction–cholestasis syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
arthrogryposis–renal dysfunction–cholestasis syndrome draws 14 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2] It is known by 12 alternative names across languages and contexts.[17]