visceral myopathy 2
MONDO:0859157Mondo
Findings
No curated finding names visceral myopathy 2 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
17 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.
- MegacystisHPOHP:0000021
- 5 of 7 reported patients
- EsophagitisHPOHP:0100633
- 5 of 8 reported patients
- Gastroesophageal refluxHPOHP:0002020
- 5 of 8 reported patients
- Hiatus herniaHPOHP:0002036
- 5 of 8 reported patients
- DysphagiaHPOHP:0002015
- 3 of 8 reported patients
- GastroparesisHPOHP:0002578
- 2 of 8 reported patients
- Ineffective esophageal peristalsisHPOHP:0031857
- 2 of 8 reported patients
- Intestinal malrotationHPOHP:0002566
- 1 of 7 reported patients
- Intestinal obstructionHPOHP:0005214
- 1 of 7 reported patients
- Rectal prolapseHPOHP:0002035
- 1 of 7 reported patients
- Barrett esophagusHPOHP:0100580
- 1 of 8 reported patients
- Chronic constipationHPOHP:0012450
- 1 of 8 reported patients
Show the remaining 5
- Esophageal strictureHPOHP:0002043
- 1 of 8 reported patients
- Intestinal pseudo-obstructionHPOHP:0004389
- 1 of 8 reported patients
- MegaduodenumHPOHP:0030996
- 1 of 8 reported patients
- Necrotizing enterocolitisHPOHP:0033165
- 1 of 8 reported patients
- VolvulusHPOHP:0002580
- 1 of 8 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.
- MYH11HGNC:7569
- Limited · Ambry Genetics · Autosomal recessive · 2024
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
Where it sits
- A kind of