neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities
Findings
No curated finding names neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
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.
- Gastrostomy tube feeding in infancyHPOHP:0011471
- 3 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 3 of 3 reported patients
- Motor delayHPOHP:0001270
- 3 of 3 reported patients
- Respiratory insufficiencyHPOHP:0002093
- 3 of 3 reported patients
- Abnormality of temperature regulationHPOHP:0004370
- 2 of 3 reported patients
- EEG abnormalityHPOHP:0002353
- 2 of 3 reported patients
- Generalized hypotoniaHPOHP:0001290
- 2 of 3 reported patients
- HyperhidrosisHPOHP:0000975
- 2 of 3 reported patients
- Neurogenic bladderHPOHP:0000011
- 2 of 3 reported patients
- Sensory neuropathyHPOHP:0000763
- 2 of 3 reported patients
- Abnormality of movementHPOHP:0100022
- 1 of 3 reported patients
- Alternating esotropiaHPOHP:0001137
- 1 of 3 reported patients
Show the remaining 14
- AmblyopiaHPOHP:0000646
- 1 of 3 reported patients
- Axial hypotoniaHPOHP:0008936
- 1 of 3 reported patients
- Cerebral visual impairmentHPOHP:0100704
- 1 of 3 reported patients
- Highly arched eyebrowHPOHP:0002553
- 1 of 3 reported patients
- HypertelorismHPOHP:0000316
- 1 of 3 reported patients
- Increased variability in muscle fiber diameterHPOHP:0003557
- 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.
- CLCN6HGNC:2024
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · G2P · Autosomal dominant · 2025
- Moderate · ClinGen · Autosomal dominant · 2026
- Limited · Ambry Genetics · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
2 names
Resolves to: neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities
- Also called
- CONRIBAneurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities