ODCs

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

PROTEIN INTERACTIONS: 1

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

Congenital muscular dystrophy with integrin alpha-7 deficiency

Congenital glaucoma


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		Congenital 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): - Congenital malformations, deformations and chromosomal abnormalities -

	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: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.