Search Ontology:
Human Disease

hypophosphatemic nephrolithiasis/osteoporosis 1

Term ID
DOID:0080077
Synonyms
Definition
A hypophosphatemic nephrolithiasis/osteoporosis that has_material_basis_in heterozygous mutation in the SLC34A1 gene on chromosome 5q35. https://www.ncbi.nlm.nih.gov/pubmed/12324554
References
Ontology
Human Disease   ( DOID:0080077 )
Relationships
is a type of
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Genes Involved
Zebrafish Models