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Familial congenital mirror movements

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
40 signs/symptoms

Familial congenital mirror movements

Bloom syndrome

DCC	(UniProt - OMIM)		BLM	(UniProt - OMIM)
RAD51	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RAD51	(0.96)	BLM

Citations in the biomedical literature:

Familial congenital mirror movements		Bloom syndrome
	Synonym(s): - Familial congenital controlateral synkinesia - Hereditary congenital controlateral synkinesia - Hereditary congenital mirror movements - Isolated congenital controlateral synkinesia - Isolated congenital mirror movements		Synonym(s): - BSyn

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare hematologic disease - Rare immune disease - Rare oncologic 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: neonatal/infancy Average age of death: adult Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D001816

Bloom syndrome
	Very frequent - Acute diarrhea - Anomalies of nose and olfaction - Anomalies of skin, subcutaneous tissue and mucosae - Autosomal recessive inheritance - Chromosome breakage - Delayed bone age - Dolichocephaly / scaphocephaly - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Flat cheek bones / malar hypoplasia - Immunodeficiency / increased susceptibility to infections / recurrent infections - Intrauterine growth retardation - Irregular / in bands / reticular skin hyperpigmentation - Narrow face - Nasal congestion / sinusitis / rhinitis / rhinorrhea - Neoplasms / tumors - Repeat respiratory infections - Short stature / dwarfism / nanism Frequent - Abnormal cry / voice / phonation disorder / nasal speech - Face / facial anomalies - Hypoplastic mandibula / partial absence of the mandibula - Short / small nose - Skin photosensitivity - Telangiectasiae of the skin Occasional - Acute leukemia - Agammaglobulinemia / hypogammaglobulinemia / B-cell deficiency - Anodontia / oligodontia / hypodontia - Digestive neoplasm / tumor / carcinoma / cancer - Failure to thrive / difficulties for feeding in infancy / growth delay - Hyperhidrosis / increased sweating - Ichthyosis / ichthyosiform dermatitis - Intellectual deficit / mental / psychomotor retardation / learning disability - Irregular / patchy skin hypopigmentation - Lymphoma - Microcephaly - Prominent / bat ears - Sacral sinus / dimple - Skin tumors / lumps / epidermal cysts - Sterility / hypofertility - Syndactyly of fingers / interdigital palm - Upper limb polydactyly / hexadactyly
Familial congenital mirror movements
(no data available)