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 blood ion concentration (HP:0003111)

Parent Node:
Abnormal blood phosphate concentration (HP:0100529)

..Starting node
..obsolete Increased urine O-phosphoethanolamine level (HP:0410158)

Term ID:

410158

Name:

obsolete Increased urine O-phosphoethanolamine level

Synonym:

Increased level of O-phosphoethanolamine in urine

Definition:

Comments:

Reference:

HP:0410158

Genes and Diseases:

Child Nodes:

Sister Nodes:

Elevated plasma pyrophosphate (HP:0011864)

Hyperphosphatemia (HP:0002905)

Hypophosphatemia (HP:0002148)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410158	HP:0410158	obsolete Increased urine O-phosphoethanolamine level	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.