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Disease association ontology term - MONDO:0013768 - arterial calcification, generalized, of infancy, 2

Term summary

ID
MONDO:0013768
Name
arterial calcification, generalized, of infancy, 2
Ontology or CV name
Disease association
Definition
Any arterial calcification of infancy in which the cause of the disease is a mutation in the ABCC6 gene.

Parents

Annotation

Disease association

MONDO:0013768 - arterial calcification, generalized, of infancy, 2

References:

Genes: