congenital hyperinsulinism
genetic disease
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congenital hyperinsulinism
Summary
congenital hyperinsulinism is a genetic disease[1]. It draws 39 Wikipedia views per month (genetic_disease category, ranking #6 of 16).[2]
Key Facts
- congenital hyperinsulinism's instance of is recorded as genetic disease[3].
- congenital hyperinsulinism's instance of is recorded as class of disease[4].
- congenital hyperinsulinism's subclass of is recorded as hyperinsulinism[5].
- congenital hyperinsulinism's subclass of is recorded as hypoglycemia[6].
- congenital hyperinsulinism's subclass of is recorded as genetic pancreatic disease[7].
- congenital hyperinsulinism's MeSH descriptor ID is recorded as D044903[8].
- congenital hyperinsulinism's OMIM ID is recorded as 256450[9].
- congenital hyperinsulinism's Freebase ID is recorded as /m/04rm1q[10].
- congenital hyperinsulinism's MeSH tree code is recorded as C06.689.150[11].
- congenital hyperinsulinism's MeSH tree code is recorded as C16.614.200[12].
- congenital hyperinsulinism's MeSH tree code is recorded as C18.452.394.968.250[13].
- congenital hyperinsulinism's MeSH tree code is recorded as C18.452.394.984.200[14].
- congenital hyperinsulinism's Orphanet ID is recorded as 657[15].
- congenital hyperinsulinism's NCI Thesaurus ID is recorded as C131425[16].
- congenital hyperinsulinism's NCI Thesaurus ID is recorded as C122923[17].
- congenital hyperinsulinism's health specialty is recorded as pediatrics[18].
- congenital hyperinsulinism's health specialty is recorded as gastroenterology[19].
- congenital hyperinsulinism's health specialty is recorded as endocrinology[20].
- congenital hyperinsulinism's BabelNet ID is recorded as 00497498n[21].
- congenital hyperinsulinism's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_657[22].
- congenital hyperinsulinism's UMLS CUI is recorded as C3888018[23].
- congenital hyperinsulinism's UMLS CUI is recorded as C0027773[24].
- congenital hyperinsulinism's UMLS CUI is recorded as C1257959[25].
- congenital hyperinsulinism's ICD-10-CM is recorded as E16.1[26].
- congenital hyperinsulinism's UK Parliament thesaurus ID is recorded as 512659[27].
Why It Matters
congenital hyperinsulinism draws 39 Wikipedia views per month (genetic_disease category, ranking #6 of 16).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] It is known by 4 alternative names across languages and contexts.[29]