ODCs

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1 OMIM reference -
3 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Retinopathy of prematurity

Autosomal dominant osteopetrosis type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NDP	(0.63)	LRP5

Citations in the biomedical literature:

Retinopathy of prematurity		Autosomal dominant osteopetrosis type 1
	Synonym(s): - ROP - Retrolental fibroplasia		Synonym(s): (no synonyms)

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D012178		External references: 1 OMIM reference - 1 MeSH reference: C536056

No signs/symptoms info available.