ODCs

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3 OMIM references -
3 associated genes
12 signs/symptoms

PROTEIN INTERACTIONS: 3

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

Multiple epiphyseal dysplasia due to collagen 9 anomaly

Autosomal dominant rhegmatogenous retinal detachment


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL9A1 COL9A3 COL9A2	(0.75) (0.62) (0.52)	COL2A1 COL2A1 COL2A1

Citations in the biomedical literature:

Multiple epiphyseal dysplasia due to collagen 9 anomaly		Autosomal dominant rhegmatogenous retinal detachment

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Multiple epiphyseal dysplasia due to collagen 9 anomaly
	Very frequent - Autosomal dominant inheritance - Epiphyseal anomaly - Osteoarthritis Frequent - Abnormal gait - Articular / joint pain / arthralgia - Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana - Joint / articular deformation - Restricted joint mobility / joint stiffness / ankylosis - Short limbs / micromelia / brachymelia - Short stature / dwarfism / nanism Occasional - Genu valgum - Genu varum
Autosomal dominant rhegmatogenous retinal detachment
(no data available)