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Hereditary arterial and articular multiple calcification syndrome
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor B-cell acute lymphoblastic leukemia
Fibronectin glomerulopathy
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
NT5E P21589129190
No signs/symptoms info available.