MCID: BNG066
MIFTS: 6

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 60
Benign Fmtle 60

Characteristics:

Orphanet epidemiological data:

60
benign familial mesial temporal lobe epilepsy
Inheritance: Autosomal dominant;

Classifications:

Orphanet: 60  
Rare neurological diseases


External Ids:

Orphanet 60 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:

42
Temporal Lobe

Publications for Benign Familial Mesial Temporal Lobe Epilepsy

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
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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