myopathy, congenital, with respiratory insufficiency and bone fractures
MONDO:0032936Mondo
Findings
No curated finding names myopathy, congenital, with respiratory insufficiency and bone fractures 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
- Death in infancy
HPO, annotations 2026-09-02
Features
11 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.
- Motor delayHPOHP:0001270
- 4 of 4 reported patients
- Neonatal hypotoniaHPOHP:0001319
- 4 of 4 reported patients
- Obstructive sleep apneaHPOHP:0002870
- 3 of 3 reported patients
- CryptorchidismHPOHP:0000028
- 1 of 3 reported patients
- ObesityHPOHP:0001513
- 1 of 3 reported patients
- Short statureHPOHP:0004322
- 1 of 3 reported patients
- AkinesiaHPOHP:0002304
- 1 of 4 reported patients
- AreflexiaHPOHP:0001284
- 1 of 4 reported patients
- OligohydramniosHPOHP:0001562
- 1 of 4 reported patients · Fetal onset
- Tongue fasciculationsHPOHP:0001308
- 1 of 4 reported patients
- EMG: myopathic abnormalitiesHPOHP:0003458
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.
- FXR1HGNC:4023
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020