Phenotype #0000015041

Individual ID	00016439
Associated disease	BWS
Phenotype details	ear abnormality (HP:0000598); abnormal kidney (HP:0000077); macrosomia (HP:0001520); macroglossia (HP:0000158); organomegaly; no abdominal wall defect (-HP:0010866); no hypoglycemia (-HP:0001943); no heart abnormality (-HP:0001627);
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Eamonn Maher
Database submission license
Created by	Johan den Dunnen
Date created	2014-04-22 17:11:31 +02:00 (CEST)
Date last edited	2020-04-07 10:37:40 +02:00 (CEST)

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