ODCs

Click node...

2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Generalized arterial calcification of infancy

Hypopigmentation-punctate palmoplantar keratoderma syndrome

ABCC6	(UniProt - OMIM)		ENPP1	(UniProt - OMIM)
ENPP1	(UniProt - OMIM)

Citations in the biomedical literature:

Generalized arterial calcification of infancy		Hypopigmentation-punctate palmoplantar keratoderma syndrome
	Synonym(s): - Idiopathic infantile arterial calcification - Idiopathic obliterative arteriopathy - Infantile arteriosclerosis - Occlusive infantile arteriopathy		Synonym(s): - Cole disease - Guttate hypopigmentation and punctate palmoplantar keratoderma - Hypopigmentation and punctate keratosis of the palms and soles

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - 1 MeSH reference: C537440		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.