ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation

Mucocutaneous venous malformations

NPHS1	(UniProt - OMIM)		TEK	(UniProt - OMIM)
PTPRO	(UniProt - OMIM)


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

Citations in the biomedical literature:

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

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

	Classification (ICD10): - Diseases of the genitourinary system -		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: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 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 diffuse mesangial proliferation
(no data available)