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Diseases

Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant

rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant

Entity Type
Diseases
Relation Groups
1
Relation Preview
5

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
Standard Disease Name
rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
C563392
OMIM ID
245570
UMLS ID
C1832814
HPO ID
No data

Description and Extensions

Description
No data
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease5 Targets
02
GRIN2A
glutamate ionotropic receptor NMDA type subunit 2A
glutamate ionotropic receptor NMDA type subunit 2A