ODCs

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

PROTEIN INTERACTIONS: 2

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

Milroy disease

Familial capillary hemangioma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLT4 VEGFC	(0.84) (0.52)	KDR KDR

Citations in the biomedical literature:

Milroy disease		Familial capillary hemangioma
	Synonym(s): - Hereditary lymphedema type I - Nonne-Milroy lymphedema		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare circulatory system disease - Rare eye disease - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - 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.