ODCs

Cytoscape Web

Click node...

Moyamoya disease

4 OMIM references -
2 associated genes
6 signs/symptoms

PROTEIN INTERACTIONS: 1

Congenital glaucoma

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

Moyamoya disease

Congenital glaucoma

ACTA2	(UniProt - OMIM)		CYP1B1	(UniProt - OMIM)
RNF213	(UniProt - OMIM)		LTBP2	(UniProt - OMIM)
			MYOC	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA2	(0.63)	MYOC

Citations in the biomedical literature:

Moyamoya disease		Congenital glaucoma

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

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

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

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
Congenital glaucoma
(no data available)