ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Congenital analbuminemia

Dermatopathia pigmentosa reticularis


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

Citations in the biomedical literature:

Congenital analbuminemia		Dermatopathia pigmentosa reticularis

	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: (no data available)

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535374

No signs/symptoms info available.