Disease #00283 (EIEE16 (encephalopathy, epileptic, early infantile, type 16 (EIEE-16)), OMIM:615338)

Official abbreviation EIEE16
Name encephalopathy, epileptic, early infantile, type 16 (EIEE-16)
OMIM ID 615338
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TBC1D24
Associated tissues -
Disease features -
Remarks -
Date created 2013-11-28 15:56:49 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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