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Congenital analbuminemia

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Naegeli-Franceschetti-Jadassohn syndrome

1 OMIM reference -
1 associated gene
6 signs/symptoms

Congenital analbuminemia

Naegeli-Franceschetti-Jadassohn syndrome

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALB	(0.72)	KRT14

Citations in the biomedical literature:

Congenital analbuminemia		Naegeli-Franceschetti-Jadassohn syndrome
	Synonym(s): (no synonyms)		Synonym(s): - NFJ syndrome - Naegeli syndrome

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive		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: No OMIM references 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
Congenital analbuminemia
(no data available)