Disease #06297 (FFEVF3 (Epilepsy, familial focal, with variable foci 3), OMIM:617118)

Official abbreviation FFEVF3
Name Epilepsy, familial focal, with variable foci 3
OMIM ID 617118
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene NPRL3
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00406434 192016 - - M ? Croatia (Hrvatska) - - - - - FFEVF3 seizure, father and brother also affected NPRL3 NPRL3 1 1 Andreas Laner
00431197 212980 - - F no Germany - - - - - FFEVF3, NS1 Seizure, Failure to thrive, Short stature, Neurodevelopmental delay NPRL3, PTPN11 NPRL3, PTPN11 2 1 Andreas Laner
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