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13 OMIM references -
14 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 3
2 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma

CACNG2 BRAF
CDH15 CTNNB1
CTNNB1
DOCK8
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


COMMON
GENES
CTNNB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TCF4
GRIN1
CDH15
(0.9)
(0.59)
(0.52)
CTNNB1
CTNNB1
CTNNB1



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Craniopharyngioma
BRAF



Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic 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:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic

External references:
13 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D003397

No signs/symptoms info available.