Central Hypoventilation Syndrome, Congenital, 3 (CCHS3)

Alias:

Cchs3

Hypoventilation, Central, Syndrome, Congenital, Type 3

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Central Hypoventilation Syndrome, Congenital, 3, is also known as cchs3. An important gene associated with Central Hypoventilation Syndrome, Congenital, 3 is LBX1 (Ladybird Homeobox 1). Affiliated tissues include lung, and related phenotypes are apnea and respiratory failure

Related ID：

MALACARDS：CNT121

OMIM：619483

MESH：D001049