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Smith-McCort dysplasia
2 OMIM references -
2 associated genes
5 connected diseases
No signs/symptoms info
Disease Type of connection
Dyggve-Melchior-Clausen disease
Familial thoracic aortic aneurysm and aortic dissection
Fibrodysplasia ossificans progressiva
Loeys-Dietz syndrome type 1
Multiple keratoacanthoma, Ferguson-Smith type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
DYM Q7RTS9607461
RAB33B Q9H082605950
No signs/symptoms info available.