Disease #04630 (BFIS2 (Seizures, benign familial infantile, type 2 (BFIS-2)), OMIM:605751)

Official abbreviation BFIS2
Name Seizures, benign familial infantile, type 2 (BFIS-2)
OMIM ID 605751
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 6
Associated with 1 gene PRRT2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00107927 - PubMed: Schubert 2012 - - - - - - - - - BFIS2 - PRRT2 PRRT2 4 1 Yvonne Weber
00151965 - - - F ? Netherlands White - - - - BFIS2 - KCNQ2, KCNQ3, PRRT2, SCN2A, TBC1D24 PRRT2 1 1 Danique Vlaskamp
00153034 - - - M - Netherlands white - - - - BFIS2 - PRRT2 PRRT2 1 1 Danique Vlaskamp
00153086 - - - F - Netherlands white - - - - BFIS2 - - PRRT2 1 1 Danique Vlaskamp
00153285 - - - F - Netherlands white - - - - BFIS2 - - PRRT2 1 1 Danique Vlaskamp
00320243 172237 - - F - - - - - - - BFIS2 benign infantile convulsions, with 4 months series of epileptic seizures, child normally developed, interectal EEG normal, family history: mother as an infant also seizures, as an adult isolated seizures PRRT2 PRRT2 1 1 Andreas Laner
00416443 203654 - - M - Germany - - - - - BFIS2 Seizure KCNQ2 KCNQ2 1 1 Andreas Laner
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