Disease #05885 (PEBEL2 (encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, type 2 (PEBEL2)), OMIM:618321)

Official abbreviation	PEBEL2
Name	encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, type 2 (PEBEL2)
OMIM ID	618321
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CARKD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-12-29 10:53:27 +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.

Global Variome shared LOVD