Phenotype #0000346143

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	00457684
Associated disease	LCHADD
Phenotype details	see paper; ..., hepatic, mother acute fatty liver of pregnancy
Diagnosis/Initial	LCHAD deficiency
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	LCHADD
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2024-11-16 11:23:45 +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.