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 metabolism/homeostasis (HP:0001939)

Parent Node:
Presence of xenobiotic (HP:0031838)

..Starting node
..Stool xenobiotic (HP:0500097)

Term ID:

500097

Name:

Stool xenobiotic

Synonym:

Definition:

Presence of xenobiotic in stool.

Comments:

Reference:

HP:0500097

Genes and Diseases:

Child Nodes:

........

Meconium xenobiotic (HP:0500098)

Sister Nodes:

Blood xenobiotic (HP:0410172)

Gastric fluid xenobiotic (HP:0500101)

Hair xenobiotic (HP:0500099)

Urine xenobiotic (HP:0031840)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500097	HP:0500097	Stool xenobiotic	0	CL E G H
HP:0500097	HP:0500098	Meconium xenobiotic	1	CL E G H
HP:0500097	HP:0410307	Positive stool methadone test	1	CL E G H
HP:0500097	HP:0410202	Positive stool barbiturate test	1	CL E G H
HP:0500097	HP:0410200	Positive meconium barbiturate test	2	CL E G H
HP:0500097	HP:0410285	Positive meconium methadone test	2	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.