myopathy, congenital proximal, with minicore lesions
MONDO:0032937Mondo
Findings
No curated finding names myopathy, congenital proximal, with minicore lesions yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
15 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.
- Neonatal hypotoniaHPOHP:0001319
- 4 of 4 reported patients · Neonatal onset
- AreflexiaHPOHP:0001284
- Centrally nucleated skeletal muscle fibersHPOHP:0003687
- CryptorchidismHPOHP:0000028
- Male
- Decreased fetal movementHPOHP:0001558
- Antenatal onset
- Fatty replacement of skeletal muscleHPOHP:0012548
- Hypoplastic male external genitaliaHPOHP:0000050
- Male
- Minicore myopathyHPOHP:0003789
- Motor delayHPOHP:0001270
- Obstructive sleep apneaHPOHP:0002870
- OligohydramniosHPOHP:0001562
- Antenatal onset
- Proximal muscle weaknessHPOHP:0003701
Show the remaining 3
- Tongue fasciculationsHPOHP:0001308
- Type 1 muscle fiber predominanceHPOHP:0003803
- Z-band streamingHPOHP:0020203
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 · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2019