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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
5 OMIM references -
8 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Familial pancreatic carcinoma

CACNG2 BRCA1
CDH15 BRCA2
CTNNB1 CDKN2A
DOCK8 KRAS
DYNC1H1 MANF
DYRK1A PALB2
EPB41L1 SMAD4
GRIN1 TP53
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
CTNNB1
DYNC1H1
(0.73)
(0.68)
(0.63)
SMAD4
BRCA1
BRCA1



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Familial pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Autosomal dominant nonsyndromic intellectual deficit
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):
(no data available)
Classification (ICD10):
- Neoplasms -

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

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

No signs/symptoms info available.