Disease #04680 (GEFSP9 (epilepsy, generalized, with febrile seizures plus, type 9 (GEFSP-9)), OMIM:616172)

Official abbreviation GEFSP9
Name epilepsy, generalized, with febrile seizures plus, type 9 (GEFSP-9)
OMIM ID 616172
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene STX1B
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

2 entries on 1 page. Showing entries 1 - 2.
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00375517 175255 - - F no - - - - - - GEFSP9 (+) Behavioral abnormality,(+) Depressivity,(+) Autistic behavior,(+) Impaired social interactions,(+) Diminished motivation,(+) Delayed speech and language development,(+) Global developmental delay,(+) Febrile seizure (within the age range of 3 months to 6 years),(+) Expressive language delay,(+) Fatigue,(+) Abnormal social behavior,(+) Neurodevelopmental abnormality,(+) Sound sensitivity,(+) Constitutional symptom,(+) Impairment in personality functioning,(+) Diminished ability to concentrate,(+) Seizure precipitated by febrile infection,(+) Abnormal emotion/affect behavior STX1B STX1B 1 1 Andreas Laner
00424212 208881 - - M - - - - - - - GEFSP9 Hyperactivity, Short attention span, Intellectual disability, Generalized-onset motor seizure, Delayed speech and language development STX1B STX1B 1 1 Andreas Laner
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