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Papilloma of choroid plexus

1 OMIM reference -
1 associated gene
10 signs/symptoms

PROTEIN INTERACTIONS: 1

Neurofibromatosis type 3

3 OMIM references -
3 associated genes
No signs/symptoms info

Papilloma of choroid plexus

Neurofibromatosis type 3

TP53	(UniProt - OMIM)		LZTR1	(UniProt - OMIM)
			NF2	(UniProt - OMIM)
			SMARCB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TP53	(0.88)	SMARCB1

Citations in the biomedical literature:

Papilloma of choroid plexus		Neurofibromatosis type 3
	Synonym(s): (no synonyms)		Synonym(s): - NF3 - Neurilemmomatosis - Schwannomatosis

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D020288		External references: 3 OMIM references - 1 MeSH reference: C536641

Papilloma of choroid plexus
	Very frequent - Autosomal recessive inheritance - Central nervous system / peripheral nerves neoplasm / tumor / carcinoma / cancer - Hydrocephaly - Structural anomalies of the nervous system Occasional - Hemiplegia / diplegia / hemiparesia / limb palsy - Hypertonia / spasticity / rigidity / stiffness - Intellectual deficit / mental / psychomotor retardation / learning disability - Mild visual loss / impaired visual acuity - Neoplasms / tumors - Seizures / epilepsy / absences / spasms / status epilepticus
Neurofibromatosis type 3
(no data available)