ODCs

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

PROTEIN INTERACTIONS: 3

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

Coppock-like cataract

Fatal infantile hypertonic myofibrillar myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CRYBB2 CRYGC CRYGD	(0.89) (0.88) (0.79)	CRYAB CRYAB CRYAB

Citations in the biomedical literature:

Coppock-like cataract		Fatal infantile hypertonic myofibrillar myopathy

	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: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

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

No signs/symptoms info available.