Disease #03114 (NPHLOP2 (nephrolithiasis/osteoporosis, hypophosphatemic, type 2 (NPHLOP-2)), OMIM:612287)

Official abbreviation NPHLOP2
Name nephrolithiasis/osteoporosis, hypophosphatemic, type 2 (NPHLOP-2)
OMIM ID 612287
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SLC9A3R1
Associated tissues -
Disease features -
Remarks -

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