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
..Projectile vomiting (HP:0002587)

Term ID:

2587

Name:

Projectile vomiting

Synonym:

Projectile vomiting

Definition:

Vomiting that ejects the gastric contents with great force.

Comments:

Reference:

HP:0002587

Genes and Diseases:

Child Nodes:

Sister Nodes:

Episodic vomiting (HP:0002572)

Feculent vomiting (HP:0025089)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0002587	HP:0002587	Projectile vomiting	0	AIMP1 CL E G H	9255	10648	OMIM:260600	Leukodystrophy, hypomyelinating, 3	.	4
HP:0002587	HP:0002587	Projectile vomiting	0	ANO1 CL E G H	55107	21625	OMIM:620045
HP:0002587	HP:0002587	Projectile vomiting	0	CLMP CL E G H	79827	24039	OMIM:615237	Congenital short bowel syndrome		7
HP:0002587	HP:0002587	Projectile vomiting	0	TIMM22 CL E G H	29928	17317	OMIM:618851	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43; COXPD43

Genes (4) :AIMP1 ANO1 CLMP TIMM22

Diseases (4) :OMIM:260600 OMIM:620045 OMIM:615237 OMIM:618851

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.