ODCs

Cytoscape Web

Click node...

Congenital analbuminemia

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 2

Epidermolysis bullosa simplex with mottled pigmentation

1 OMIM reference -
2 associated genes
10 signs/symptoms

Congenital analbuminemia

Epidermolysis bullosa simplex with mottled pigmentation

ALB	(UniProt - OMIM)		KRT14	(UniProt - OMIM)
			KRT5	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALB ALB	(0.72) (0.72)	KRT14 KRT5

Citations in the biomedical literature:

Congenital analbuminemia		Epidermolysis bullosa simplex with mottled pigmentation
	Synonym(s): (no synonyms)		Synonym(s): - EBS-MP

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - 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: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535959

Epidermolysis bullosa simplex with mottled pigmentation
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Autosomal dominant inheritance - Follicular / erythematous / edematous papules / milium - Irregular / patchy skin hypopigmentation - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Abnormal fingernails - Bruisability - Nails anomalies - Palmoplantar hyperkeratosis / keratoderma - Premature ageing
Congenital analbuminemia
(no data available)