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Phakomatosis pigmentokeratotica

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Follicular lymphoma

1 OMIM reference -
4 associated genes
14 signs/symptoms

Phakomatosis pigmentokeratotica

Follicular lymphoma

HRAS	(UniProt - OMIM)		BCL2	(UniProt - OMIM)
			BCL6	(UniProt - OMIM)
			HLA-DRB1	(UniProt - OMIM)
			IGH	(UniProt)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HRAS	(0.52)	BCL2

Citations in the biomedical literature:

Phakomatosis pigmentokeratotica		Follicular lymphoma

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare hematologic 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: 1-5 / 10 000 Average age onset: adulthood Average age of death: adult Type of inheritance: multigenic/multifactorial

	External references: No OMIM references 1 MeSH reference: C537893		External references: 1 OMIM reference - 1 MeSH reference: D008224

Follicular lymphoma
	Very frequent - Fever / chilling - Hematologic / blood / lymphatic cancer - Hyperhidrosis / increased sweating - Lymphadenopathy / polyadenopathies - Weight loss / loss of appetite / break in weight curve / general health alteration Frequent - Asthenia / fatigue / weakness - Mediastinal / hilar adenopathies - Splenomegaly Occasional - Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax - Anomalies of skin, subcutaneous tissue and mucosae - Bone marrow / medullar infiltration - Lymphedema - Meningitis / meningeal syndrome - Structural anomaly of the peritoneum
Phakomatosis pigmentokeratotica
(no data available)