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MCID: BNG066
MIFTS: 7
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Benign Familial Mesial Temporal Lobe Epilepsy
Categories:
Genetic diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Benign Familial Mesial Temporal Lobe Epilepsy:
Name: Benign Familial Mesial Temporal Lobe Epilepsy
58
Characteristics:Orphanet epidemiological data:58
benign familial mesial temporal lobe epilepsy
Inheritance: Autosomal dominant; Classifications:
Orphanet: 58
Rare neurological diseases External Ids:
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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.
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MalaCards organs/tissues related to Benign Familial Mesial Temporal Lobe Epilepsy:40
Temporal Lobe
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Articles related to Benign Familial Mesial Temporal Lobe Epilepsy:
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Search
GEO
for disease gene expression data for Benign Familial Mesial Temporal Lobe Epilepsy.
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