ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Renal tubular dysgenesis of genetic origin

LMNA-related cardiocutaneous progeria syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACE	(0.49)	LMNA

Citations in the biomedical literature:

Renal tubular dysgenesis of genetic origin		LMNA-related cardiocutaneous progeria syndrome
	Synonym(s): (no synonyms)		Synonym(s): - LCPS

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

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

No signs/symptoms info available.