ODCs

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2 OMIM references -
4 associated genes
6 signs/symptoms

PROTEIN INTERACTIONS: 3

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

Idiopathic juvenile osteoporosis

Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DKK1 WNT1 WNT3A	(0.89) (0.85) (0.84)	LRP6 LRP6 LRP6

Citations in the biomedical literature:

Idiopathic juvenile osteoporosis		Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis
	Synonym(s): - IJO - Juvenile osteoporosis		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Idiopathic juvenile osteoporosis
	Very frequent - Bone pain - Mutiple fractures / bone fragility - Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets Frequent - Abnormal gait - Motor deficit / trouble Occasional - Kyphosis
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis
(no data available)