ODCs

Cytoscape Web

Click node...

Autosomal recessive centronuclear myopathy

1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Moyamoya disease

4 OMIM references -
2 associated genes
6 signs/symptoms

Autosomal recessive centronuclear myopathy

Moyamoya disease

BIN1	(UniProt - OMIM)		ACTA2	(UniProt - OMIM)
TTN	(UniProt - OMIM)		RNF213	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TTN	(0.55)	ACTA2

Citations in the biomedical literature:

Autosomal recessive centronuclear myopathy		Moyamoya disease
	Synonym(s): - AR-CNM		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - 2 MeSH references: C536991 / D009072

Moyamoya disease
	Very frequent - Autosomal recessive inheritance - Vascular anomalies of skin / mucosae Frequent - Cerebral vascular anomalies - Dilated cerebral ventricles without hydrocephaly - Intellectual deficit / mental / psychomotor retardation / learning disability - Seizures / epilepsy / absences / spasms / status epilepticus
Autosomal recessive centronuclear myopathy
(no data available)