Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal urinary electrolyte concentration (HP:0012591)

Parent Node:
Abnormal urine magnesium concentration (HP:0012607)

..Starting node
..Hypomagnesiuria (HP:0012609)

Term ID:

12609

Name:

Hypomagnesiuria

Synonym:

Decreased urine magnesium; Low urine magnesium levels

Definition:

An decreased concentration of magnesium the urine.

Comments:

Reference:

HP:0012609

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hypermagnesiuria (HP:0012608)

Renal magnesium wasting (HP:0005567)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012609	HP:0012609	Hypomagnesiuria	0	CL E G H

Genes (0) :

Diseases (0) :

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