ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
3 associated genes
No signs/symptoms info

Congenital lethal myopathy, Compton-North type

Generalized pseudohypoaldosteronism type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CNTN1	(0.62)	SCNN1B

Citations in the biomedical literature:

Congenital lethal myopathy, Compton-North type		Generalized pseudohypoaldosteronism type 1
	Synonym(s): (no synonyms)		Synonym(s): - Autosomal recessive pseudohypoaldosteronism type 1

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.