Phenotype #0000340095

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	00109437
Associated disease	CTLN1
Phenotype details	symptomatic hyperammonemia
Diagnosis/Initial	citrullinemia
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	CTLN1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	00y00m03d
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2024-05-31 14:55:16 +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.