ODCs

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4 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Osteogenesis imperfecta type 2

Kufor-Rakeb syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL1A1	(0.72)	ATP13A2

Citations in the biomedical literature:

Osteogenesis imperfecta type 2		Kufor-Rakeb syndrome
	Synonym(s): - Lethal osteogenesis imperfecta - OI type 2		Synonym(s): - PARK9

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.