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Familial congenital mirror movements

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

PROTEIN INTERACTIONS: 1

Mantle cell lymphoma

3 associated genes
7 signs/symptoms

Familial congenital mirror movements

Mantle cell lymphoma

DCC	(UniProt - OMIM)		ATM	(UniProt - OMIM)
RAD51	(UniProt - OMIM)		CCND1	(UniProt - OMIM)
			IGH	(UniProt)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RAD51	(0.74)	ATM

Citations in the biomedical literature:

Familial congenital mirror movements		Mantle cell lymphoma
	Synonym(s): - Familial congenital controlateral synkinesia - Hereditary congenital controlateral synkinesia - Hereditary congenital mirror movements - Isolated congenital controlateral synkinesia - Isolated congenital mirror movements		Synonym(s): - LCM - MCL - Mantle zone lymphoma

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

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

	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: 1-9 / 100 000 Average age onset: adulthood Average age of death: adult Type of inheritance: multigenic/multifactorial

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references 1 MeSH reference: D020522

Mantle cell lymphoma
	Very frequent - Hematologic / blood / lymphatic cancer - Lymphadenopathy / polyadenopathies Frequent - Anorexia - Asthenia / fatigue / weakness - Bone marrow / medullar infiltration - Splenomegaly - Weight loss / loss of appetite / break in weight curve / general health alteration
Familial congenital mirror movements
(no data available)