Wolcott-Rallison syndrome
Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure
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Wolcott-Rallison syndrome
Summary
Wolcott-Rallison syndrome is a rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Wolcott-Rallison syndrome's instance of is recorded as rare disease[3].
- Wolcott-Rallison syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Wolcott-Rallison syndrome's instance of is recorded as class of disease[5].
- Wolcott-Rallison syndrome is a type of autosomal recessive disease[6].
- Wolcott-Rallison syndrome is a type of developmental anomaly of metabolic origin[7].
- Wolcott-Rallison syndrome is a type of other rare diabetes mellitus[8].
- Wolcott-Rallison syndrome is a type of rare genetic diabetes mellitus[9].
- Wolcott-Rallison syndrome is a type of syndrome[10].
- Wolcott-Rallison syndrome's Commons category is recorded as Wolcott–Rallison syndrome[11].
- Wolcott-Rallison syndrome's symptoms and signs is recorded as hepatic insufficiency[12].
- Wolcott-Rallison syndrome's NCI Thesaurus ID is recorded as C131007[13].
- Wolcott-Rallison syndrome's genetic association is recorded as EIF2AK3[14].
- Wolcott-Rallison syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090060[15].
- Wolcott-Rallison syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090060[16].
- Wolcott-Rallison syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1667[17].
- Wolcott-Rallison syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Wolcott-Rallison syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[19]