cardioacrofacial dysplasia 2
MONDO:0030877Mondo
Findings
No curated finding names cardioacrofacial dysplasia 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
25 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.
- Postaxial hand polydactylyHPOHP:0001162
- 4 of 4 reported patients
- Common atriumHPOHP:0011565
- 3 of 4 reported patients · Congenital onset
- Postaxial foot polydactylyHPOHP:0001830
- 3 of 4 reported patients
- BrachydactylyHPOHP:0001156
- 2 of 4 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 2 of 4 reported patients
- Genu valgumHPOHP:0002857
- 2 of 4 reported patients
- HypodontiaHPOHP:0000668
- 2 of 4 reported patients
- Long faceHPOHP:0000276
- 2 of 4 reported patients
- Long thoraxHPOHP:0100818
- 2 of 4 reported patients
- Narrow chestHPOHP:0000774
- 2 of 4 reported patients
- Accessory oral frenulumHPOHP:0000191
- 1 of 4 reported patients
- Atrioventricular canal defectHPOHP:0006695
- 1 of 4 reported patients
Show the remaining 13
- Broad foreheadHPOHP:0000337
- 1 of 4 reported patients
- ClubbingHPOHP:0001217
- 1 of 4 reported patients
- Conical toothHPOHP:0000698
- 1 of 4 reported patients
- Deep philtrumHPOHP:0002002
- 1 of 4 reported patients
- HypertelorismHPOHP:0000316
- 1 of 4 reported patients
- Left superior vena cava draining to coronary sinusHPOHP:0011670
- 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.
- PRKACBHGNC:9381
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Strong · G2P · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
2 names
Resolves to: cardioacrofacial dysplasia 2
- Also called
- CAFD2cardioacrofacial dysplasia 2, autosomal dominant, somatic mosaicism