Phenotype #0000274674

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	00380821
Associated disease	MRXSBL;MRX60
Phenotype details	ID; cerebellar hypoplasia (Neurological)
Diagnosis/Initial	-
Inheritance	Familial
Diagnosis/Definite	X-linked mental retardation with cerebellar hypoplasia
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Birth_Details	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-08-23 12:15:23 +02:00 (CEST)
Date last edited	N/A

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