Disease #06620 (EIEE40 (?Epileptic encephalopathy, early infantile, 40), OMIM:617065)

Official abbreviation EIEE40
Name ?Epileptic encephalopathy, early infantile, 40
OMIM ID 617065
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GUF1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +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.