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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Squamous cell carcinoma of head and neck

CACNG2 ING1
CDH15 ING3
CTNNB1 PTEN
DOCK8 TNFRSF10B
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.49)
PTEN



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Squamous cell carcinoma of head and neck
ING1 ING3 PTEN TNFRSF10B



Autosomal dominant nonsyndromic intellectual deficit
Squamous cell carcinoma of head and neck

Synonym(s):
(no synonyms)

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

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

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

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:
1 OMIM reference -
1 MeSH reference: C535575

No signs/symptoms info available.