ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
5 signs/symptoms

Unverricht-Lundborg disease

Hereditary cerebral hemorrhage with amyloidosis, Icelandic type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSTB	(0.65)	CST3

Citations in the biomedical literature:

Unverricht-Lundborg disease		Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
	Synonym(s): - Progressive myoclonic epilepsy type 1 - ULD		Synonym(s): - HCHWA, Icelandic type - Hereditary cystatin C amyloid angiopathy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood 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: 3 OMIM references - 1 MeSH reference: D020194		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
Unverricht-Lundborg disease
(no data available)