Search Ontology:
Human Disease

hypophosphatemic nephrolithiasis/osteoporosis 2

Term ID
DOID:0080078
Synonyms
Definition
A hypophosphatemic nephrolithiasis/osteoporosis that has_material_basis_in heterozygous mutation in the SLC9A3R1 gene on chromosome 17q25.1. (3)
References
Ontology
Human Disease   ( DOID:0080078 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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