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Squamous cell carcinoma of head and neck
1 OMIM reference -
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
Squamous cell carcinoma of head and neck
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

ING1
(UniProt - OMIM)
 APP
(UniProt - OMIM)
ING3
(UniProt - OMIM)
PTEN
(UniProt - OMIM)
TNFRSF10B
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ING3
(0.56)
APP


Citations in the biomedical literature:


Squamous cell carcinoma of head and neck
ING1 ING3 PTEN TNFRSF10B
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Squamous cell carcinoma of head and neck
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C535575
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.