FEB9
MCID: FBR067
MIFTS: 15

Febrile Seizures, Familial, 9 (FEB9)

Categories: Genetic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Febrile Seizures, Familial, 9

MalaCards integrated aliases for Febrile Seizures, Familial, 9:

Name: Febrile Seizures, Familial, 9 56 13
Feb9 56 12
Febrile Convulsions, Familial, 9; Feb9 56
Febrile Convulsions, Familial, 9 56
Familial Febrile Convulsions 9 12
Familial Febrile Seizures 9 12

Characteristics:

OMIM:

56
Inheritance:
autosomal dominant

Miscellaneous:
febrile seizures show onset between 6 months and 3 years
febrile seizures remit by age 5 or 6
absence seizures show onset between 3.5 and 4 years
absence seizures usually remit by puberty


HPO:

31
febrile seizures, familial, 9:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

Disease Ontology 12 DOID:0111303
OMIM 56 611634
OMIM Phenotypic Series 56 PS121210
MedGen 41 C1968846

Summaries for Febrile Seizures, Familial, 9

Disease Ontology : 12 A familial febrile seizures that has material basis in variation in a region on chromosome 3p24.2-p23.

MalaCards based summary : Febrile Seizures, Familial, 9, also known as feb9, is related to familial febrile seizures. An important gene associated with Febrile Seizures, Familial, 9 is FEB9 (Febrile Convulsions, Familial, 9). Related phenotypes are absence seizure and febrile seizures

More information from OMIM: 611634 PS121210

Related Diseases for Febrile Seizures, Familial, 9

Diseases in the Febrile Seizures family:

Febrile Seizures, Familial, 1 Febrile Seizures, Familial, 2
Febrile Seizures, Familial, 4 Febrile Seizures, Familial, 8
Febrile Seizures, Familial, 6 Febrile Seizures, Familial, 5
Febrile Seizures, Familial, 7 Febrile Seizures, Familial, 9
Febrile Seizures, Familial, 10 Febrile Seizures, Familial, 11
Familial Febrile Seizures

Diseases related to Febrile Seizures, Familial, 9 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 familial febrile seizures 11.3

Symptoms & Phenotypes for Febrile Seizures, Familial, 9

Human phenotypes related to Febrile Seizures, Familial, 9:

31
# Description HPO Frequency HPO Source Accession
1 absence seizure 31 HP:0002121
2 febrile seizures 31 HP:0002373
3 eeg with spike-wave complexes (>3.5 hz) 31 HP:0010849

Symptoms via clinical synopsis from OMIM:

56
Neurologic Central Nervous System:
febrile seizures
childhood absence seizures
eeg shows 3-hz spike-wave discharges

Clinical features from OMIM:

611634

Drugs & Therapeutics for Febrile Seizures, Familial, 9

Search Clinical Trials , NIH Clinical Center for Febrile Seizures, Familial, 9

Genetic Tests for Febrile Seizures, Familial, 9

Anatomical Context for Febrile Seizures, Familial, 9

Publications for Febrile Seizures, Familial, 9

Articles related to Febrile Seizures, Familial, 9:

# Title Authors PMID Year
1
New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p. 56
17452582 2007

Variations for Febrile Seizures, Familial, 9

Expression for Febrile Seizures, Familial, 9

Search GEO for disease gene expression data for Febrile Seizures, Familial, 9.

Pathways for Febrile Seizures, Familial, 9

GO Terms for Febrile Seizures, Familial, 9

Sources for Febrile Seizures, Familial, 9

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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