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:
Abnormal urinary sulfate concentration (HP:0012612)

..Starting node
..Increased urinary sulfate (HP:0012613)

Term ID:

12613

Name:

Increased urinary sulfate

Synonym:

Increased urinary sulphate

Definition:

Elevated concentration of SO4(2-), i.e., sulfate, in the urine.

Comments:

Reference:

HP:0012613

Genes and Diseases:

Child Nodes:

Sister Nodes:

Decreased urinary sulfate (HP:0003359)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012613	HP:0012613	Increased urinary sulfate	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.