Phenotype #0000288141

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Pia Ostergaard, Michel van Geel, Élodie Fastré, and Pascal Brouillard

Individual ID	00394942
Associated disease	XLHR
Phenotype details	bone deformities, longitudinal growth retardation (≤2 SD),
Diagnosis/Initial	hypophosphatemic rickets
Inheritance	Unknown
Diagnosis/Definite	XLHR
Age/Examination	-
Age/Diagnosis	2y1m
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2021-12-02 16:30:25 +01:00 (CET)
Date last edited	N/A

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