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Tall stature - scoliosis - macrodactyly of the great toes
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Acromesomelic dysplasia, Maroteaux type
Familial atrial fibrillation
Synonym(s):
- Tall stature - scoliosis - macrodactyly of the halluces

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

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
NPR2 P20594108961
No signs/symptoms info available.