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Typical nemaline myopathy

5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Papilloma of choroid plexus

1 OMIM reference -
1 associated gene
10 signs/symptoms

Typical nemaline myopathy

Papilloma of choroid plexus

ACTA1	(UniProt - OMIM)		TP53	(UniProt - OMIM)
CFL2	(UniProt - OMIM)
KLHL41	(UniProt - OMIM)
NEB	(UniProt - OMIM)
TPM2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.52)	TP53

Citations in the biomedical literature:

Typical nemaline myopathy		Papilloma of choroid plexus

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D020288

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
Typical nemaline myopathy
(no data available)