Phenotype #0000291955

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00398857
Associated disease	OBAIRH
Phenotype details	see paper; ..., early-onset obesity, red hair, hypocortisolism, hypoglycemia, convulsions
Diagnosis/Initial	hypoglycemia, convulsions
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	OBAIRH
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	hypoglycemia, convulsions
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-01-13 17:19:20 +01:00 (CET)
Date last edited	N/A

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