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English
familial temporal lobe epilepsy 6
temporal lobe epilepsy that has material basis in variation in the chromosome region 3q25-q26
ETL6
EPILEPSY, FAMILIAL TEMPORAL LOBE, 6; ETL6
EPILEPSY, FAMILIAL TEMPORAL LOBE, 6
familial temporal lobe epilepsy type 6
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Statements
instance of
class of disease
0 references
subclass of
temporal lobe epilepsy
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060749
genetic disease
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:0060749
autosomal dominant disease
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060749
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0060749
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060749
http://identifiers.org/doid/DOID:0060749
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
Disease Ontology ID
DOID:0060749
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060749
Mondo ID
MONDO_0014308
0 references
OMIM ID
615697
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060749
615697
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0014308
Orphanet ID
163717
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060749
UMLS CUI
C3810320
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0014308
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