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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement

APP CLDN16


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
CLDN16



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

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- FHHNC without severe ocular involvement
- HOMG3
- Renal hypomagnesemia type 3

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

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

Epidemiological data:
(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

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)