Phenotype #0000239313

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00315557
Associated disease	HSCR
Diagnosis/Initial	Hirschsprung disease
Diagnosis/Definite	-
Phenotype details	see paper; ..., Hirschsprung disease, heterochromia iridum
Inheritance	Familial, autosomal dominant
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Veronique Pingault
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2020-10-28 09:10:48 +01:00 (CET)
Date last edited	N/A

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