Neurodevelopmental Disorder with Microcephaly, Impaired Language, Epilepsy, and Gait Abnormalities (NEDMILEG)

Alias:

Nedmileg

Neurodevelopmental Disorder with Microcephaly, Impaired Language, Epilepsy, and Gait Abnormalities, Autosomal Dominant

Neurodevelopmental Disorder with Microcephaly, Impaired Language, Epilepsy, Gait Abnormalities, Autosomal Dominant

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Neurodevelopmental Disorder with Microcephaly, Impaired Language, Epilepsy, and Gait Abnormalities, is also known as nedmileg. An important gene associated with Neurodevelopmental Disorder with Microcephaly, Impaired Language, Epilepsy, and Gait Abnormalities is NARS1 (Asparaginyl-TRNA Synthetase 1). Affiliated tissues include brain, and related phenotypes are intellectual disability and ataxia

Related ID：

MALACARDS：NRD113

OMIM：619092

MESH：D065886