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Pseudohypoaldosteronism type 2E

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
14 signs/symptoms

Pseudohypoaldosteronism type 2E

Perry syndrome

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUL3	(0.63)	DCTN1

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Perry syndrome
	Synonym(s): - PHA2E		Synonym(s): - Parkinsonism with alveolar hypoventilation and mental depression

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

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

Perry syndrome
	Very frequent - Autosomal dominant inheritance - Execution movement disorder / dysmetria / bradykinesia / akinesia / apraxia - Extrapyramidal syndrome - Humour troubles / anxiety / depression / apathy / euphoria / irritability - Respiratory distress / dyspnea / respiratory failure / lung volume reduction - Sleep and vigilance disorders - Tremor - Weight loss / loss of appetite / break in weight curve / general health alteration Occasional - Delirium / hallucination - Early death / lethality - Hypotension - Psychic / behavioural troubles - Psychic / psychomotor regression / dementia / intellectual decline - Psychosis / schizophrenia / maniac disorder
Pseudohypoaldosteronism type 2E
(no data available)