ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

CLOVE syndrome

Unclassified chronic myeloproliferative disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PIK3CA	(0.52)	PDGFRB

Citations in the biomedical literature:

CLOVE syndrome		Unclassified chronic myeloproliferative disease
	Synonym(s): - Congenital lipomatous overgrowth - vascular malformation - epidermal nevi		Synonym(s): - CMPD-U - Undifferentiated myeloproliferative disease

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic		Epidemiological data: (no data available)

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

No signs/symptoms info available.