intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
MONDO:0044318Mondo
Findings
No curated finding names intellectual developmental disorder with gastrointestinal difficulties and high pain threshold 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
33 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.
- HyperacusisHPOHP:0010780
- 7 of 7 reported patients
- Intellectual disabilityHPOHP:0001249
- 13 of 14 reported patients
- Small handHPOHP:0200055
- 10 of 11 reported patients
- Short footHPOHP:0001773
- 7 of 8 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 10 of 12 reported patients
- Posteriorly rotated earsHPOHP:0000358
- 8 of 10 reported patients
- Gastroesophageal refluxHPOHP:0002020
- 10 of 13 reported patients
- Short statureHPOHP:0004322
- 9 of 12 reported patients
- Feeding difficultiesHPOHP:0011968
- 10 of 14 reported patients
- HypotoniaHPOHP:0001252
- 10 of 14 reported patients
- HyperlordosisHPOHP:0003307
- 7 of 10 reported patients
- Low-set earsHPOHP:0000369
- 7 of 10 reported patients
Show the remaining 21
- Broad foreheadHPOHP:0000337
- 8 of 12 reported patients
- ConstipationHPOHP:0002019
- 8 of 13 reported patients
- Recurrent infectionsHPOHP:0002719
- 5 of 9 reported patients
- Broad-based gaitHPOHP:0002136
- 5 of 10 reported patients
- Small nailHPOHP:0001792
- 6 of 12 reported patients
- StrabismusHPOHP:0000486
- 7 of 14 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.
- PPM1DHGNC:9277
- Definitive · G2P · Autosomal dominant · 2016
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2017
Where it sits
Other names
1 name
Resolves to: intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
- Also called
- Jansen de Vries syndrome