Disease #02394 (HHF2 (hypoglycemia, hyperinsulinemic, familial, type 2 (HHF-2)), OMIM:601820)

Official abbreviation HHF2
Name hypoglycemia, hyperinsulinemic, familial, type 2 (HHF-2)
OMIM ID 601820
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene KCNJ11
Associated tissues -
Disease features autosomal recessive
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00306129 62 - - F - China - - - - - HHF2 - KCNJ11 KCNJ11 2 1 Sha Hong
00306217 119 - - M - China - - - - - HHF2 - KCNJ11 KCNJ11 1 1 Sha Hong
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