ZFIN Human Disease: familial hyperinsulinemic hypoglycemia 1

OBO ID: DOID:0070219

Term Name:	familial hyperinsulinemic hypoglycemia 1		Search Ontology:
Synonyms:	HHF1
Definition:	A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has_material_basis_in mutation in the ABCC8 gene on chromosome 11p15. (3)
References:	OMIM:256450
Ontology:	Human Disease ( DOID:0070219 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease hyperinsulinemic hypoglycemia autosomal dominant disease autosomal recessive disease hyperinsulinemic hypoglycemia Show first 5 Terms

OTHER familial hyperinsulinemic hypoglycemia 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ABCC8	abcc8b abcc8	Hyperinsulinemic hypoglycemia, familial, 1	256450

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None