Phenotype #0000357047

Individual ID	00472238
Associated disease	PWS
Phenotype details	0001511: Intrauterine growth retardation, 001531: Growth retardation in infants, 0001319: Neonatal hypotonia, 0001290: Generalised hypotonia, 0008872: Eating disorders in children
Diagnosis/Initial	Congenital myopathy
Inheritance	Isolated (sporadic)
Diagnosis/Definite	PWS
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Camille Verebi
Database submission license
Created by	Camille Verebi
Date created	2026-01-19 16:23:11 +01:00 (CET)
Date last edited	2026-02-06 11:32:21 +01:00 (CET)

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