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Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

CLDN16
(UniProt - OMIM)
 APP
(UniProt - OMIM)

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
CLDN16
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- FHHNC without severe ocular involvement
- HOMG3
- Renal hypomagnesemia type 3
Synonym(s):
- HCHWA, Flemish 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
No signs/symptoms info available.