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:
Nausea and vomiting (HP:0002017)

Parent Node:
Vomiting (HP:0002013)

..Starting node
..Feculent vomiting (HP:0025089)

Term ID:

25089

Name:

Feculent vomiting

Synonym:

Faecal vomiting; Fecal vomiting; Stercoraceous vomiting; Vomiting faecal matter; Vomiting fecal matter

Definition:

Vomiting of material that is of fecal origin.

Comments:

Reference:

HP:0025089

Genes and Diseases:

Child Nodes:

Sister Nodes:

Episodic vomiting (HP:0002572)

Projectile vomiting (HP:0002587)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025089	HP:0025089	Feculent vomiting	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.