ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Rare isolated myopia

X-linked intellectual deficit, Porteous type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SCO2	(0.49)	PQBP1

Citations in the biomedical literature:

Rare isolated myopia		X-linked intellectual deficit, Porteous type

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

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.