Disease #03638 (FEB11 (Febrile seizures, familial, 11), OMIM:614418)

Official abbreviation FEB11
Name Febrile seizures, familial, 11
OMIM ID 614418
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene CPA6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00206725 - - - F yes France Moroccan - - - - FEB11 - CPA6 CPA6 1 1 Annick Salzmann
00206726 - - - F yes France Moroccan - - - - ETL5, FEB11 - CPA6 CPA6 1 1 Annick Salzmann
00206727 - - - F yes France Moroccan - - - - FEB11 Photosensitivity CPA6 CPA6 1 1 Annick Salzmann
00206728 - - - M yes France Moroccan - - - - FEB11 Mental retardation CPA6 CPA6 1 1 Annick Salzmann
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