short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1
MONDO:0100297Mondo
Findings
No curated finding names short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 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
24 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.
- Anteverted naresHPOHP:0000463
- 12 of 12 reported patients
- Long philtrumHPOHP:0000343
- 12 of 12 reported patients
- Short noseHPOHP:0003196
- 12 of 12 reported patients
- Midface retrusionHPOHP:0011800
- 11 of 12 reported patients
- Sandal gapHPOHP:0001852
- 8 of 11 reported patients
- Short statureHPOHP:0004322
- 8 of 11 reported patients
- 11 pairs of ribsHPOHP:0000878
- 6 of 9 reported patients
- Broad foreheadHPOHP:0000337
- 8 of 12 reported patients
- Dental crowdingHPOHP:0000678
- 6 of 10 reported patients
- Posteriorly rotated earsHPOHP:0000358
- 7 of 12 reported patients
- SynophrysHPOHP:0000664
- 5 of 9 reported patients
- Anterior open-bite malocclusionHPOHP:0009102
- 5 of 10 reported patients
Show the remaining 12
- Clinodactyly of the 5th fingerHPOHP:0004209
- 4 of 11 reported patients
- Conductive hearing impairmentHPOHP:0000405
- 4 of 11 reported patients
- Obstructive sleep apneaHPOHP:0002870
- 4 of 11 reported patients
- ArrhythmiaHPOHP:0011675
- 3 of 9 reported patients
- SpondylolisthesisHPOHP:0003302
- 3 of 9 reported patients
- Everted lower lip vermilionHPOHP:0000232
- 2 of 7 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.
- BMP2HGNC:1069
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · G2P · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025