ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement

Hereditary cerebral hemorrhage with amyloidosis, Arctic type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CLDN16	(0.56)	APP

Citations in the biomedical literature:

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement		Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Synonym(s): - FHHNC without severe ocular involvement - HOMG3 - Renal hypomagnesemia type 3		Synonym(s): - HCHWA, Arctic type

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

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

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Very frequent - Autosomal dominant inheritance - Psychic / behavioural troubles - Psychic / psychomotor regression / dementia / intellectual decline
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
(no data available)