Disease #01863 (LIH (Hypoglycemia of infancy, leucine-sensitive), OMIM:240800)

Official abbreviation LIH
Name Hypoglycemia of infancy, leucine-sensitive
OMIM ID 240800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ABCC8
Associated tissues -
Disease features -
Remarks -