ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Familial congenital mirror movements

Xeroderma pigmentosum complementation group D

DCC	(UniProt - OMIM)		ERCC2	(UniProt - OMIM)
RAD51	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RAD51	(0.52)	ERCC2

Citations in the biomedical literature:

Familial congenital mirror movements		Xeroderma pigmentosum complementation group D
	Synonym(s): - Familial congenital controlateral synkinesia - Hereditary congenital controlateral synkinesia - Hereditary congenital mirror movements - Isolated congenital controlateral synkinesia - Isolated congenital mirror movements		Synonym(s): - XPD

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

	Classification (ICD10): (no data available)		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 dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.