Human Phenotype Ontology 
Grandparent Node:
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Abnormal circulating calcium concentration (HP:0004363)help
Grandparent Node:
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Abnormal urinary electrolyte concentration (HP:0012591)help
Parent Node:
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Abnormality of urine calcium concentration (HP:0011280)help
..Starting node
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Hypocalciuria (HP:0003127)help
Term ID: 3127
Name: Hypocalciuria
Synonym: Low urine calcium levels
Definition: An abnormally decreased calcium concentration in the urine.
Comments:
Reference: HP:0003127
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHypercalciuria (HP:0002150) help
..expandReduced ratio of renal calcium clearance to creatinine clearance (HP:0003513) help
..expandRenal calcium wasting (HP:0012637) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003127HP:0003127Hypocalciuria0AP2S1 CL E G H1175565OMIM:600740Hypocalciuric hypercalcemia, familial, type III.6
HP:0003127HP:0003127Hypocalciuria0CASR CL E G H8461514OMIM:145980Hypocalciuric hypercalcemia, familial, type I.272
HP:0003127HP:0003127Hypocalciuria0CLCNKB CL E G H11882027OMIM:607364Bartter syndrome, type 3HP:0040283 - Occasional27
HP:0003127HP:0003127Hypocalciuria0CLDN10 CL E G H90712033OMIM:617671Helix syndrome.3
HP:0003127HP:0003127Hypocalciuria0FAM20A CL E G H5475723015ORPHA:1031Enamel-renal syndromeHP:0040282 - Frequent16
HP:0003127HP:0003127Hypocalciuria0FXYD2 CL E G H4864026OMIM:154020Hypomagnesemia 2, renal.17
HP:0003127HP:0003127Hypocalciuria0GNA11 CL E G H27674379OMIM:145981Hypocalciuric hypercalcemia, familial, type II.16
HP:0003127HP:0003127Hypocalciuria0KCNJ10 CL E G H37666256OMIM:612780Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance.121
HP:0003127HP:0003127Hypocalciuria0PHEX CL E G H52518918ORPHA:89936X-linked hypophosphatemiaHP:0040281 - Very frequent217
HP:0003127HP:0003127Hypocalciuria0SLC12A3 CL E G H655910912OMIM:263800Gitelman syndrome.145


Genes (10) :AP2S1 CASR CLCNKB CLDN10 FAM20A FXYD2 GNA11 KCNJ10 PHEX SLC12A3

Diseases (10) :OMIM:600740 OMIM:145980 OMIM:607364 OMIM:617671 ORPHA:1031 OMIM:154020 OMIM:145981 OMIM:612780 ORPHA:89936 OMIM:263800
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.