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Familial osteochondritis dissecans
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Spondyloepimetaphyseal dysplasia, aggrecan type
Spondyloepiphyseal dysplasia, Kimberley type
Nodulosis-arthropathy-osteolysis syndrome
Torg-Winchester syndrome
Wagner disease
Synpolydactyly type 2
Hypomaturation amelogenesis imperfecta
Severe generalized recessive dystrophic epidermolysis bullosa
Synonym(s):
- Osteochondritis dissecans and short stature
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ACAN P16112155760
No signs/symptoms info available.