Seizures, Benign Familial Infantile, 1 (BFIS1)

Alias:

Benign Familial Neonatal-Infantile Seizures 1

Convulsions, Benign Familial Infantile, 1

Benign Familial Infantile Seizures, 1

Benign Familial Infantile Seizures 1

Familial Benign Neonatal Epilepsy

Bfis1

Bfic1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Seizures, Benign Familial Infantile, 1, also known as benign familial neonatal-infantile seizures 1, is related to seizures, benign familial neonatal, 1 and seizures, benign familial infantile, 2, and has symptoms including cyanosis An important gene associated with Seizures, Benign Familial Infantile, 1 is BFIS1 (Benign Familial Infantile Convulsions). Affiliated tissues include eye, and related phenotypes are apnea and cyanosis

Related ID：

MALACARDS：SZR014

OMIM：601764