spondyloepimetaphyseal dysplasia, Krakow type
MONDO:0032571Mondo
Findings
No curated finding names spondyloepimetaphyseal dysplasia, Krakow type 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
- Congenital onset
HPO, annotations 2026-09-02
Features
37 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.
- 2-3 toe syndactylyHPOHP:0004691
- 2 of 2 reported patients
- Allergic rhinitisHPOHP:0003193
- 2 of 2 reported patients
- AsthmaHPOHP:0002099
- 2 of 2 reported patients
- BrachydactylyHPOHP:0001156
- 2 of 2 reported patients
- Bruising susceptibilityHPOHP:0000978
- 2 of 2 reported patients
- Chiari malformationHPOHP:0002308
- 2 of 2 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 2 of 2 reported patients
- Decreased circulating IgM concentrationHPOHP:0002850
- 2 of 2 reported patients
- Decreased circulating insulin-like growth factor 1 concentrationHPOHP:0030353
- 1 of 1 reported patient
- Delayed pubic bone ossificationHPOHP:0008788
- 2 of 2 reported patients
- Eczematoid dermatitisHPOHP:0000964
- 2 of 2 reported patients
- Elbow contractureHPOHP:0034391
- 2 of 2 reported patients
Show the remaining 25
- Elevated circulating alkaline phosphatase concentrationHPOHP:0003155
- 2 of 2 reported patients
- Frontal bossingHPOHP:0002007
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- High palateHPOHP:0000218
- 2 of 2 reported patients
- HypertelorismHPOHP:0000316
- 2 of 2 reported patients
- ImmunodeficiencyHPOHP:0002721
- 2 of 2 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.
- SIK3HGNC:29165
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2020
Where it sits
- A kind of