Compton-North congenital myopathy
MONDO:0012929Mondo
Findings
No curated finding names Compton-North congenital myopathy 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
- Infantile onset · Neonatal onset
HPO, annotations 2026-09-02
Features
10 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.
- Decreased fetal movementHPOHP:0001558
- 4 of 4 reported patients
- HypotoniaHPOHP:0001252
- 16 of 16 reported patients
- Muscle weaknessHPOHP:0001324
- 16 of 16 reported patients
- Premature birthHPOHP:0001622
- 4 of 4 reported patients
- Jaw contractureHPOHP:0033333
- 4 of 16 reported patients
- AreflexiaHPOHP:0001284
- 2 of 16 reported patients
- Feeding difficultiesHPOHP:0011968
- 2 of 16 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 16 reported patients
- Pulmonary artery stenosisHPOHP:0004415
- 1 of 16 reported patients
- Abnormal circulating creatine kinase activityHPOHP:0040081
- 0 of 7 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.
- CNTN1HGNC:2171
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
- Moderate · Ambry Genetics · Autosomal recessive · 2020
- Supportive · Orphanet · Autosomal recessive · 2021