neuromuscular disease and ocular or auditory anomalies with or without seizures
MONDO:0032890Mondo
Findings
No curated finding names neuromuscular disease and ocular or auditory anomalies with or without seizures 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
32 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.
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Generalized hypotoniaHPOHP:0001290
- 2 of 4 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 4 reported patients
- AreflexiaHPOHP:0001284
- 1 of 4 reported patients
- AspirationHPOHP:0002835
- 1 of 4 reported patients
- Bilateral tonic-clonic seizureHPOHP:0002069
- 1 of 4 reported patients
- Calf muscle hypertrophyHPOHP:0008981
- 1 of 4 reported patients
- Chorioretinal lacunaeHPOHP:0007858
- 1 of 4 reported patients
- Elevated circulating creatine kinase activityHPOHP:0003236
- 1 of 4 reported patients
- EMG: myopathic abnormalitiesHPOHP:0003458
- 1 of 4 reported patients
- EpicanthusHPOHP:0000286
- 1 of 4 reported patients
- Infantile spasmsHPOHP:0012469
- 1 of 4 reported patients
Show the remaining 20
- Knee flexion contractureHPOHP:0006380
- 1 of 4 reported patients
- Multiple renal cystsHPOHP:0005562
- 1 of 4 reported patients
- Muscle fiber necrosisHPOHP:0003713
- 1 of 4 reported patients
- Peripheral hypomyelinationHPOHP:0007182
- 1 of 4 reported patients
- Poor head controlHPOHP:0002421
- 1 of 4 reported patients
- Posteriorly rotated earsHPOHP:0000358
- 1 of 4 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.
- DHX16HGNC:2739
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2024
- Limited · G2P · Autosomal dominant · 2025
Where it sits
- A kind of