Central Hypoventilation Syndrome, Congenital, 1 (CCHS1)

Central Hypoventilation Syndrome, Congenital, 1(来自ICD-11)

别称:

Central Hypoventilation Syndrome, Congenital, 1, with or Without Hirschsprung Disease

Cchs

Central Hypoventilation Syndrome, Congenital

Congenital Failure of Autonomic Control

Hypoventilation

Cchs1

Hypoventilation, Central, Syndrome, Congenital, with/without Hirschsprung Disease

Central Hypoventilation Syndrome, Congenital, 1, with or Without Hirschsprung

Hypoventilation, Central, Syndrome, Congenital, Type 1

Congenital Central Alveolar Hypoventilation Syndrome

Central Alveolar Hypoventilation Syndrome

Autonomic Control, Congenital Failure of

Congenital Central Hypoventilation

Sleep-Related Respiratory Failure

Cchs with Hirschsprung Disease

Ondine Curse, Congenital

Sleep Apnea, Central

Ondine Curse

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Central Hypoventilation Syndrome, Congenital, 1, also known as cchs, is related to neuroblastoma 2 and congenital central hypoventilation syndrome, and has symptoms including apnea, constipation and increased sweating. An important gene associated with Central Hypoventilation Syndrome, Congenital, 1 is PHOX2B (Paired Like Homeobox 2B), and among its related pathways/superpathways are Sudden infant death syndrome (SIDS) susceptibility pathways and Neural Stem Cells and Lineage-specific Markers. The drugs Opium and Acetazolamide have been mentioned in the context of this disorder. Affiliated tissues include lung and heart, and related phenotypes are hypoventilation and central hypoventilation

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