Disease #02599 (HHF6 (Hyperinsulinism-hyperammonemia syndrome), OMIM:606762)

Official abbreviation HHF6
Name Hyperinsulinism-hyperammonemia syndrome
OMIM ID 606762
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GLUD1
Associated tissues -
Disease features -
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

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00451650 3bINP-085 PubMed: Vela-Amieva 2024 Familial case. Co-occurrence of two different monogenic diseases M no Mexico Mexican - - - - HHF6 Hypoglicemia, Hyperammonemia. Co-ocorrence of Hemolytic anemia, G6PD deficient (favism) (OMIM: 300908) GLUD1 G6PD, GLUD1 3 1 Miriam Erandi Reyna-Fabián
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