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Autosomal dominant rhegmatogenous retinal detachment
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Legg-Calvé-Perthes disease
1 OMIM reference -
1 associated gene
9 signs/symptoms
Autosomal dominant rhegmatogenous retinal detachment
Legg-Calvé-Perthes disease

COL2A1
(UniProt - OMIM)
 COL2A1
(UniProt - OMIM)

COMMON
GENES 		COL2A1


Citations in the biomedical literature:


Autosomal dominant rhegmatogenous retinal detachment
COL2A1
Legg-Calvé-Perthes disease



Autosomal dominant rhegmatogenous retinal detachment
Legg-Calvé-Perthes disease

Synonym(s):
(no synonyms)

Synonym(s):
- Aseptic necrosis of the capital femoral epiphysis
- Osteochondritis of the capital femoral epiphysis
- Osteochondrosis of the capital femoral epiphysis
- Perthes disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
Legg-Calvé-Perthes disease

Very frequent
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Articular / joint pain / arthralgia
- Cartilage destruction / chondrolysis
- Delayed bone age
- Joint / articular deformation
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Osteonecrosis / bone infarction
- Polygenic / multifactorial inheritance
- Short stature / dwarfism / nanism



Autosomal dominant rhegmatogenous retinal detachment

(no data available)