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 sternum morphology (HP:0000766)

Parent Node:
Abnormality of the xiphoid process (HP:0100892)

..Starting node
..Prominent xiphoid process (HP:0100893)

Term ID:

100893

Name:

Prominent xiphoid process

Synonym:

Prominent xiphisternum

Definition:

Increased prominence of the xiphoid process of the sternum.

Comments:

Reference:

HP:0100893

Genes and Diseases:

Child Nodes:

Sister Nodes:

Bifid xiphoid process (HP:0100891)

Broad xiphoid process (HP:0100894)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100893	HP:0100893	Prominent xiphoid process	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.