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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
8 associated genes
No signs/symptoms info
Distal 16p11.2 microdeletion syndrome
Familial pancreatic carcinoma

SH2B1 BRCA1
BRCA2
CDKN2A
KRAS
MANF
PALB2
SMAD4
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SH2B1
(0.63)
BRCA1



Citations in the biomedical literature:


Distal 16p11.2 microdeletion syndrome
SH2B1
Familial pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Distal 16p11.2 microdeletion syndrome
Familial pancreatic carcinoma

Synonym(s):
- Distal del(16)(p11.2)
- Distal monosomy 16p11.2

Synonym(s):
- Familial pancreatic cancer

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.