ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Glaucoma secondary to spherophakia/ectopia lentis and megalocornea

Hereditary sensorimotor neuropathy with hyperelastic skin


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LTBP2	(0.7)	FBLN5

Citations in the biomedical literature:

Glaucoma secondary to spherophakia/ectopia lentis and megalocornea		Hereditary sensorimotor neuropathy with hyperelastic skin
	Synonym(s): - Megalocornea - spherophakia - secondary glaucoma		Synonym(s): (no synonyms)

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

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

	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 / 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: No OMIM references No MeSH references

No signs/symptoms info available.