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1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
7 signs/symptoms
Squamous cell carcinoma of head and neck
Hereditary cerebral hemorrhage with amyloidosis, Italian type

ING1 APP
ING3
PTEN
TNFRSF10B


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, Italian type
APP



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

Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma

Synonym(s):
- HCHWA, Italian 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

Hereditary cerebral hemorrhage with amyloidosis, Italian type

Very frequent
- Autosomal dominant inheritance
- Facial pain / cephalalgia / migraine
- Intracranial / cerebral / meningeal hemorrhage
- Transient cerebral ischemia / stroke

Frequent
- Obnubilation / coma / lethargia / desorientation
- Psychic / psychomotor regression / dementia / intellectual decline
- Seizures / epilepsy / absences / spasms / status epilepticus



Squamous cell carcinoma of head and neck

(no data available)