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 sodium concentration (HP:0012603)

..Starting node
..Hyponatriuria (HP:0012604)

Term ID:

12604

Name:

Hyponatriuria

Synonym:

Low urine sodium levels

Definition:

An abnormally decreased sodium concentration in the urine.

Comments:

Reference:

HP:0012604

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hypernatriuria (HP:0012605)

Renal sodium wasting (HP:0012606)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012604	HP:0012604	Hyponatriuria	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.