central hypoventilation syndrome, congenital, 2, and autonomic dysfunction
MONDO:0030537Mondo
Findings
No curated finding names central hypoventilation syndrome, congenital, 2, and autonomic dysfunction yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Neonatal onset
HPO, annotations 2026-09-02
Features
26 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- AchalasiaHPOHP:0002571
- 3 of 3 reported patients
- ApneaHPOHP:0002104
- 3 of 3 reported patients
- Chronic constipationHPOHP:0012450
- 3 of 3 reported patients
- DysphagiaHPOHP:0002015
- 3 of 3 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 3 reported patients · Neonatal onset
- Gait disturbanceHPOHP:0001288
- 2 of 2 reported patients
- Gastrostomy tube feeding in infancyHPOHP:0011471
- 3 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- HypopneaHPOHP:0040213
- 3 of 3 reported patients · Neonatal onset
- HypoventilationHPOHP:0002791
- 3 of 3 reported patients · Neonatal onset
- Ineffective esophageal peristalsisHPOHP:0031857
- 3 of 3 reported patients
- Small intestinal dysmotilityHPOHP:0012850
- 3 of 3 reported patients
Show the remaining 14
- SeizureHPOHP:0001250
- 2 of 3 reported patients
- AreflexiaHPOHP:0001284
- 1 of 3 reported patients
- Aspiration pneumoniaHPOHP:0011951
- 1 of 3 reported patients
- AstigmatismHPOHP:0000483
- 1 of 3 reported patients
- Gastroesophageal refluxHPOHP:0002020
- 1 of 3 reported patients
- HypotoniaHPOHP:0001252
- 1 of 3 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- HGNC:13879HGNC:13879
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2021
- Limited · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
1 name
Resolves to: central hypoventilation syndrome, congenital, 2, and autonomic dysfunction
- Also called
- CCHS2