intellectual developmental disorder with short stature and variable skeletal anomalies
MONDO:0032759Mondo
Findings
No curated finding names intellectual developmental disorder with short stature and variable skeletal anomalies 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
9 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.
- CamptodactylyHPOHP:0012385
- Clinodactyly of the 5th fingerHPOHP:0004209
- Delayed speech and language developmentHPOHP:0000750
- DysarthriaHPOHP:0001260
- DyskinesiaHPOHP:0100660
- Overlapping toeHPOHP:0001845
- Severe intellectual disabilityHPOHP:0010864
- Short statureHPOHP:0004322
- Short thumbHPOHP:0009778
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.
- WIPI2HGNC:32225
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2019
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
Where it sits
- A kind of