Phenotype #0000290722

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Individual ID	00397598
Associated disease	dysplasia, bone
Diagnosis/Initial	hypophosphatemic rickets
Diagnosis/Definite	XLHR
Phenotype details	see paper; ...
Inheritance	Isolated (sporadic)
Age/Examination	10m
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2021-12-27 11:55:19 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.