Disease #02429 (HHF3 (hypoglycemia, hyperinsulinemic, familial, type 3 (HHF-3)), OMIM:602485)

Official abbreviation HHF3
Name hypoglycemia, hyperinsulinemic, familial, type 3 (HHF-3)
OMIM ID 602485
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GCK
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     
ID_report     
Reference     
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Age at death     
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Disease     
Phenotype details     
Genes screened
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Owner     
00295607 - - - - - - - - - - - HHF3, NIDDM ORPHA:79299 HP:0005978 HP:0008283 HP:0001988 HP:0001985 HP:0000825 GCK GCK 1 4 Fanny Kortüm
00375526 179529 - - M ? Turkey - - - - - HHF3 MODY, glucosuria, elevated fasting glucose 103 mg/dl, 2h value in OGTT 109 mg/dl GCK GCK 1 1 Andreas Laner
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