ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Pseudohypoaldosteronism type 2E

Naegeli-Franceschetti-Jadassohn syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUL3	(0.63)	KRT14

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Naegeli-Franceschetti-Jadassohn syndrome
	Synonym(s): - PHA2E		Synonym(s): - NFJ syndrome - Naegeli syndrome

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

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

Naegeli-Franceschetti-Jadassohn syndrome
	Very frequent - Autosomal dominant inheritance - Dysplastic / thick / grooved fingernails - Dysplastic / thick / grooved toenails - Enamel anomaly - Irregular / in bands / reticular skin hyperpigmentation - Palmoplantar hyperkeratosis / keratoderma
Pseudohypoaldosteronism type 2E
(no data available)