MCID: BNG066
MIFTS: 7

Benign Familial Mesial Temporal Lobe Epilepsy

Categories: Genetic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Benign Familial Mesial Temporal Lobe Epilepsy

MalaCards integrated aliases for Benign Familial Mesial Temporal Lobe Epilepsy:

Name: Benign Familial Mesial Temporal Lobe Epilepsy 59
Benign Fmtle 59

Characteristics:

Orphanet epidemiological data:

59
benign familial mesial temporal lobe epilepsy
Inheritance: Autosomal dominant;

Classifications:

Orphanet: 59  
Rare neurological diseases


External Ids:

Orphanet 59 ORPHA163717

Summaries for Benign Familial Mesial Temporal Lobe Epilepsy

MalaCards based summary : Benign Familial Mesial Temporal Lobe Epilepsy, is also known as benign fmtle. An important gene associated with Benign Familial Mesial Temporal Lobe Epilepsy is CPA6 (Carboxypeptidase A6). Affiliated tissues include temporal lobe.

Related Diseases for Benign Familial Mesial Temporal Lobe Epilepsy

Symptoms & Phenotypes for Benign Familial Mesial Temporal Lobe Epilepsy

Drugs & Therapeutics for Benign Familial Mesial Temporal Lobe Epilepsy

Search Clinical Trials , NIH Clinical Center for Benign Familial Mesial Temporal Lobe Epilepsy

Genetic Tests for Benign Familial Mesial Temporal Lobe Epilepsy

Anatomical Context for Benign Familial Mesial Temporal Lobe Epilepsy

MalaCards organs/tissues related to Benign Familial Mesial Temporal Lobe Epilepsy:

41
Temporal Lobe

Publications for Benign Familial Mesial Temporal Lobe Epilepsy

Articles related to Benign Familial Mesial Temporal Lobe Epilepsy:

# Title Authors PMID Year
1
Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26. 38
24315020 2014
2
Longitudinal MRI volumetric evaluation in patients with familial mesial temporal lobe epilepsy. 38
21431086 2011
3
Evidence of memory impairment in asymptomatic individuals with hippocampal atrophy. 38
15582848 2004

Variations for Benign Familial Mesial Temporal Lobe Epilepsy

Expression for Benign Familial Mesial Temporal Lobe Epilepsy

Search GEO for disease gene expression data for Benign Familial Mesial Temporal Lobe Epilepsy.

Pathways for Benign Familial Mesial Temporal Lobe Epilepsy

GO Terms for Benign Familial Mesial Temporal Lobe Epilepsy

Sources for Benign Familial Mesial Temporal Lobe Epilepsy

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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