Phenotype #0000272737

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	00377583
Associated disease	DFNB22
Phenotype details	-
Diagnosis/Initial	Hearing loss
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	DFNB22
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Maria Pia Leone
Database submission license	No license selected
Created by	Maria Pia Leone
Date created	2021-07-28 10:50:45 +02:00 (CEST)
Date last edited	2021-08-18 14:31:16 +02:00 (CEST)

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