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
Press Enter · cited answer in seconds
0 sources
Wolcott-Rallison syndrome
Summary
Wolcott-Rallison syndrome is a rare disease[1]. It draws 10 Wikipedia views per month (rare_disease category, ranking #228 of 627).[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's subclass of is recorded as autosomal recessive disease[6].
- Wolcott-Rallison syndrome's subclass of is recorded as developmental anomaly of metabolic origin[7].
- Wolcott-Rallison syndrome's subclass of is recorded as other rare diabetes mellitus[8].
- Wolcott-Rallison syndrome's subclass of is recorded as rare genetic diabetes mellitus[9].
- Wolcott-Rallison syndrome's subclass of is recorded as syndrome[10].
- Wolcott-Rallison syndrome's Commons category is recorded as Wolcott–Rallison syndrome[11].
- Wolcott-Rallison syndrome's MeSH descriptor ID is recorded as C536739[12].
- Wolcott-Rallison syndrome's OMIM ID is recorded as 226980[13].
- Wolcott-Rallison syndrome's KEGG ID is recorded as H00766[14].
- Wolcott-Rallison syndrome's Disease Ontology ID is recorded as DOID:0090060[15].
- Wolcott-Rallison syndrome's symptoms and signs is recorded as hepatic insufficiency[16].
- Wolcott-Rallison syndrome's Orphanet ID is recorded as 1667[17].
- Wolcott-Rallison syndrome's NCI Thesaurus ID is recorded as C131007[18].
- Wolcott-Rallison syndrome's genetic association is recorded as EIF2AK3[19].
- Wolcott-Rallison syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090060[20].
- Wolcott-Rallison syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090060[21].
- Wolcott-Rallison syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1667[22].
- Wolcott-Rallison syndrome's UMLS CUI is recorded as C0432217[23].
- Wolcott-Rallison syndrome's ICD-10-CM is recorded as E13[24].
- Wolcott-Rallison syndrome's GARD rare disease ID is recorded as 5589[25].
- Wolcott-Rallison syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[26].
- Wolcott-Rallison syndrome's Mondo ID is recorded as MONDO_0009192[27].
Why It Matters
Wolcott-Rallison syndrome draws 10 Wikipedia views per month (rare_disease category, ranking #228 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 8 alternative names across languages and contexts.[29]