ODCs

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

PROTEIN INTERACTIONS: 1

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

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy

Hypohidrotic ectodermal dysplasia with immunodeficiency

MYO6	(UniProt - OMIM)		IKBKG	(UniProt - OMIM)
			NFKBIA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYO6	(0.72)	IKBKG

Citations in the biomedical literature:

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy		Hypohidrotic ectodermal dysplasia with immunodeficiency
	Synonym(s): - Progressive neurosensory deafness - hypertrophic cardiomyopathy - Progressive neurosensory hearing loss - hypertrophic cardiomyopathy - Progressive sensorineural deafness - hypertrophic cardiomyopathy		Synonym(s): - Anhidrotic ectodermal dysplasia with immunodeficiency - EDA-ID - HED-ID

	Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease - Rare skin disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: autosomal dominant

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

No signs/symptoms info available.