(Q54553148)

English

early infantile epileptic encephalopathy 19

human disease

EIEE19
Epileptic Encephalopathy, Early Infantile, type 19
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19

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Statements

1 reference

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome

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infantile epileptic encephalopathy

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genetic association

2 references

UniProt protein ID

13 August 2019

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome

NCI Thesaurus ID

C142802

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http://www.orpha.net/ORDO/Orphanet_33069

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Identifiers

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

UniProt disease ID

0 references

Sitelinks

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