ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial primary hypomagnesemia with normocalcuria and normocalcemia

LMNA-related cardiocutaneous progeria syndrome

CNNM2	(UniProt - OMIM)		LMNA	(UniProt - OMIM)
EGF	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EGF	(0.67)	LMNA

Citations in the biomedical literature:

Familial primary hypomagnesemia with normocalcuria and normocalcemia		LMNA-related cardiocutaneous progeria syndrome
	Synonym(s): (no synonyms)		Synonym(s): - LCPS

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant		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: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.