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Phakomatosis pigmentokeratotica
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Craniopharyngioma
2 associated genes
No signs/symptoms info
Phakomatosis pigmentokeratotica
Craniopharyngioma

HRAS
(UniProt - OMIM)
 BRAF
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HRAS
(0.78)
BRAF


Citations in the biomedical literature:


Phakomatosis pigmentokeratotica
HRAS
Craniopharyngioma
BRAF CTNNB1



Phakomatosis pigmentokeratotica
Craniopharyngioma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
1 MeSH reference: C537893
External references:
No OMIM references
1 MeSH reference: D003397
No signs/symptoms info available.