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:
Abnormality of urine homeostasis (HP:0003110)

Parent Node:
Abnormality of urine bicarbonate level (HP:0011279)

..Starting node
..Decreased urine bicarbonate concentration (HP:0045011)

Term ID:

45011

Name:

Decreased urine bicarbonate concentration

Synonym:

Decreased urine HCO3 concentration

Definition:

Abnormally decreased concentration of hydrogencarbonate in the urine.

Comments:

Reference:

HP:0045011

Genes and Diseases:

Child Nodes:

Sister Nodes:

Bicarbonaturia (HP:0003646)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0045011	HP:0045011	Decreased urine bicarbonate concentration	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.