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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
Hypochondrogenesis
Familial avascular necrosis of femoral head

COL2A1 COL2A1


COMMON
GENES
COL2A1



Citations in the biomedical literature:


Hypochondrogenesis
COL2A1
Familial avascular necrosis of femoral head



Hypochondrogenesis
Familial avascular necrosis of femoral head

Synonym(s):
(no synonyms)

Synonym(s):
- Familial osteonecrosis of the femoral head

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- 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: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
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.