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Hereditary sensory and autonomic neuropathy type 1
4 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

ATL1
(UniProt - OMIM)
 APP
(UniProt - OMIM)
ATL3
(UniProt - OMIM)
SPTLC1
(UniProt - OMIM)
SPTLC2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ATL3
(0.56)
APP


Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 1
ATL1 ATL3 SPTLC1 SPTLC2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Hereditary sensory and autonomic neuropathy type 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Flemish type
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):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.