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1 OMIM reference -
1 associated gene
12 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Spondyloepimetaphyseal dysplasia, Missouri type
Nodulosis-arthropathy-osteolysis syndrome

MMP13 MMP14
MMP2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MMP13
(0.52)
MMP14



Citations in the biomedical literature:


Spondyloepimetaphyseal dysplasia, Missouri type
MMP13
Nodulosis-arthropathy-osteolysis syndrome
MMP14 MMP2



Spondyloepimetaphyseal dysplasia, Missouri type
Nodulosis-arthropathy-osteolysis syndrome

Synonym(s):
- SEMD type 2
- SEMD, Missouri type
- Spondyloepimetaphyseal dysplasia type 2

Synonym(s):
- Multicentric osteolysis - nodulosis - arthropathy
- NAO syndrome

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references

Spondyloepimetaphyseal dysplasia, Missouri type

Very frequent
- Abnormal vertebral size / shape
- Autosomal dominant inheritance
- Bowed diaphysis / diaphyses / long bones
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Epiphyseal anomaly
- Metaphyseal anomaly

Frequent
- Genu varum
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Osteoarthritis
- Rhizomelic micromelia
- Short stature / dwarfism / nanism

Occasional
- Restricted joint mobility / joint stiffness / ankylosis


Nodulosis-arthropathy-osteolysis syndrome

(no data available)