ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
10 signs/symptoms

Congenital lethal myopathy, Compton-North type

Liddle syndrome

CNTN1	(UniProt - OMIM)		SCNN1B	(UniProt - OMIM)
			SCNN1G	(UniProt - OMIM)


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		Liddle syndrome
	Synonym(s): (no synonyms)		Synonym(s): - Pseudoaldosteronism - Pseudohyperaldosteronism type 1

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the circulatory 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: childhood Average age of death: adult Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D056929

Liddle syndrome
	Very frequent - Autosomal dominant inheritance - Cardiac rhythm disorder / arrhythmia - Chronic arterial hypertension - Constipation - Hypokalemia Frequent - Asthenia / fatigue / weakness - Muscle weakness / flaccidity - Renal disease / nephropathy - Renal failure - Transient cerebral ischemia / stroke
Congenital lethal myopathy, Compton-North type
(no data available)