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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
5 signs/symptoms
CLN10 disease
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type

CTSD CST3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTSD
(0.52)
CST3



Citations in the biomedical literature:


CLN10 disease
CTSD
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
CST3



CLN10 disease
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type

Synonym(s):
- Cathepsin D deficiency

Synonym(s):
- HCHWA, Icelandic type
- Hereditary cystatin C amyloid angiopathy

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

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

Hereditary cerebral hemorrhage with amyloidosis, Icelandic type

Very frequent
- Autosomal dominant inheritance
- Cerebral vascular anomalies
- Intracranial / cerebral / meningeal hemorrhage
- Transient cerebral ischemia / stroke

Occasional
- Early death in adulthood


CLN10 disease

(no data available)