Disease #04342 (DEE29 (encephalopathy, developmental and epileptic, type 29 (DEE29)), OMIM:616339)

Official abbreviation DEE29
Name encephalopathy, developmental and epileptic, type 29 (DEE29)
OMIM ID 616339
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene AARS
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2020-12-18 13:48:43 +01:00 (CET)

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