ODCs

Click node...

1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Mucocutaneous venous malformations

Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TEK	(0.68)	PTPRO

Citations in the biomedical literature:

Mucocutaneous venous malformations		Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
	Synonym(s): - Cutaneous and mucosal venous malformation - VMCM		Synonym(s): (no synonyms)

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

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

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

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

Mucocutaneous venous malformations
	Very frequent - Arteriovenous malformations / vascular malformations (excluding port-wine stains) - Autosomal dominant inheritance - Vascular anomalies of skin / mucosae
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
(no data available)