ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Neurofibromatosis type 3

Hereditary cerebral hemorrhage with amyloidosis, Arctic type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SMARCB1	(0.56)	APP

Citations in the biomedical literature:

Neurofibromatosis type 3		Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Synonym(s): - NF3 - Neurilemmomatosis - Schwannomatosis		Synonym(s): - HCHWA, Arctic type

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - 1 MeSH reference: C536641		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
Neurofibromatosis type 3
(no data available)