Disease #00097

Official abbreviation FIME
Name epilepsy, myoclonic, infantile, familial (FIME)
OMIM ID 605021
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene TBC1D24
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00004091 - PubMed: Falace A et al 2010 Falace A et al. Am J Hum Genet 2010; 87(3): 365-70. - - - Italian - 0 - - FIME - TBC1D24 TBC1D24 2 1 Philippe Campeau
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