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Generalized arterial calcification of infancy
2 OMIM references -
2 associated genes
9 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal recessive hypophosphatemic rickets
Hypopigmentation-punctate palmoplantar keratoderma syndrome
Pseudoxanthoma elasticum
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Leprechaunism
Rabson-Mendenhall syndrome
Amyotrophic lateral sclerosis
Reticular dysgenesis
Synonym(s):
- Idiopathic infantile arterial calcification
- Idiopathic obliterative arteriopathy
- Infantile arteriosclerosis
- Occlusive infantile arteriopathy
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
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
External references:
2 OMIM references -
1 MeSH reference: C537440
Gene symbol UniProt reference OMIM reference
ABCC6 O95255603234
ENPP1 P22413173335
No signs/symptoms info available.