An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the atp-binding cassette transporter gene abcc8, both on chromosome 11. [ MESH:D046768 ]
Synonyms: persistent hyperinsulinemia hypoglycemia of infancy hyperinsulinemia hypoglycemia islet cell hyperplasia hyperinsulinemic hypoglycemia (disease)
Term information
- Orphanet:443095 (MONDO:equivalentTo)
- DOID:13317 (MONDO:equivalentTo)
- NANDO:2200399 (https://orcid.org/0000-0003-0011-764X)
- SCTID:42681006 (MONDO:equivalentTo)
- HP:0000825 (MONDO:otherHierarchy)
- OMIMPS:256450 (MONDO:equivalentTo)
- NANDO:2100143 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:351247 (MONDO:equivalentTo)
- NCIT:C4375 (MONDO:relatedTo)
- EFO:0007318 (MONDO:equivalentTo)
- GARD:21849 (MONDO:GARD)
- UMLS:C1864903 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders
http://linkedlifedata.com/resource/umls/id/C1864903
http://www.orpha.net/ORDO/Orphanet_443095
http://identifiers.org/snomedct/42681006
http://purl.obolibrary.org/obo/DOID_13317
https://omim.org/phenotypicSeries/PS256450
http://identifiers.org/medgen/351247