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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
5 OMIM references -
8 associated genes
No signs/symptoms info
Severe congenital nemaline myopathy
Familial pancreatic carcinoma

ACTA1 BRCA1
KLHL40 BRCA2
KLHL41 CDKN2A
NEB KRAS
MANF
PALB2
SMAD4
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACTA1
ACTA1
(0.63)
(0.52)
CDKN2A
TP53



Citations in the biomedical literature:


Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB
Familial pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Severe congenital nemaline myopathy
Familial pancreatic carcinoma

Synonym(s):
(no synonyms)

Synonym(s):
- Familial pancreatic cancer

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
5 OMIM references -
1 MeSH reference: C535837

No signs/symptoms info available.