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Disease association ontology term - MONDO:0012676 - autosomal recessive osteopetrosis 4

Term summary

ID
MONDO:0012676
Name
autosomal recessive osteopetrosis 4
Ontology or CV name
Disease association
Definition
Any autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the CLCN7 gene.

Parents

Annotation

Disease association

MONDO:0012676 - autosomal recessive osteopetrosis 4

References:

Genes: