short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2
MONDO:0030953Mondo
Findings
No curated finding names short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Antenatal onset
HPO, annotations 2026-09-02
Features
39 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.
- High foreheadHPOHP:0000348
- 15 of 15 reported patients
- Long faceHPOHP:0000276
- 14 of 14 reported patients
- Postnatal growth retardationHPOHP:0008897
- 15 of 15 reported patients
- Short chinHPOHP:0000331
- 14 of 14 reported patients
- Triangular faceHPOHP:0000325
- 14 of 14 reported patients
- Long noseHPOHP:0003189
- 13 of 15 reported patients
- Prominent nasal bridgeHPOHP:0000426
- 13 of 15 reported patients
- Pointed chinHPOHP:0000307
- 11 of 13 reported patients
- BrachydactylyHPOHP:0001156
- 12 of 15 reported patients
- Dental crowdingHPOHP:0000678
- 12 of 15 reported patients
- Short palmHPOHP:0004279
- 12 of 15 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 8 of 11 reported patients
Show the remaining 27
- MicrocephalyHPOHP:0000252
- 9 of 13 reported patients
- Short long boneHPOHP:0003026
- 6 of 11 reported patients
- Thick vermilion borderHPOHP:0012471
- 7 of 15 reported patients
- ScoliosisHPOHP:0002650
- 6 of 13 reported patients
- Joint stiffnessHPOHP:0001387
- 3 of 8 reported patients
- 11 pairs of ribsHPOHP:0000878
- 4 of 13 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.
- SCUBE3HGNC:13655
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal recessive · 2021
- Moderate · Ambry Genetics · Autosomal recessive · 2021
Where it sits
Other names
1 name
Resolves to: short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2
- Also called
- SSFSC2