ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

6 OMIM references -
2 associated genes
No signs/symptoms info

Congenital muscular dystrophy with integrin alpha-7 deficiency

Juvenile glaucoma

ITGA7	(UniProt - OMIM)		CYP1B1	(UniProt - OMIM)
			MYOC	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ITGA7	(0.63)	MYOC

Citations in the biomedical literature:

Congenital muscular dystrophy with integrin alpha-7 deficiency		Juvenile glaucoma
	Synonym(s): - Congenital muscular dystrophy with ITGA7 deficiency		Synonym(s): (no synonyms)

	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 nervous system -		Classification (ICD10): (no data available)

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

	External references: 1 OMIM reference - No MeSH references		External references: 6 OMIM references - No MeSH references

No signs/symptoms info available.