(Q56002605)

English

adult familial myoclonic epilepsy 3

human disease

EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3
Cortical Myoclonic Tremor With Epilepsy, Familial, 3
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3
familial adult myoclonic epilepsy 3

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instance of

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subclass of

benign adult familial myoclonic epilepsy

1 reference

29 November 2020

autosomal dominant disease

1 reference

29 November 2020

http://www.orpha.net/ORDO/Orphanet_86814

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http://purl.obolibrary.org/obo/DOID_0111695

1 reference

29 November 2020

http://identifiers.org/doid/DOID:0111695

1 reference

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https://registry.identifiers.org/registry/doid

Identifiers

1 reference

29 November 2020

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mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

(Q56002605)

adult familial myoclonic epilepsy 3

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