ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial avascular necrosis of femoral head

Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis

Citations in the biomedical literature:

Familial avascular necrosis of femoral head		Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis
	Synonym(s): - Familial osteonecrosis of the femoral head		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.