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Familial congenital mirror movements

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

PROTEIN INTERACTIONS: 1

Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

Familial congenital mirror movements

Familial hypospadias

DCC	(UniProt - OMIM)		AR	(UniProt - OMIM)
RAD51	(UniProt - OMIM)		MAMLD1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DCC	(0.79)	AR

Citations in the biomedical literature:

Familial congenital mirror movements		Familial hypospadias
	Synonym(s): - Familial congenital controlateral synkinesia - Hereditary congenital controlateral synkinesia - Hereditary congenital mirror movements - Isolated congenital controlateral synkinesia - Isolated congenital mirror movements		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital 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: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 4 OMIM references - No MeSH references

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Familial congenital mirror movements
(no data available)