Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 thorax morphology (HP:0000765)

Parent Node:
Abnormal sternum morphology (HP:0000766)

..Starting node
..Abnormality of the xiphoid process (HP:0100892)

Term ID:

100892

Name:

Abnormality of the xiphoid process

Synonym:

Definition:

An abnormality of the xiphoid process of the sternum.

Comments:

Reference:

HP:0100892

Genes and Diseases:

Child Nodes:

........

Bifid xiphoid process (HP:0100891)

........

Prominent xiphoid process (HP:0100893)

........

Broad xiphoid process (HP:0100894)

Sister Nodes:

Abnormal sternal ossification (HP:0011863)

Aplasia/Hypoplasia of the sternum (HP:0006714)

Bifid sternum (HP:0010309)

Bulging of the costochondral junction (HP:0000893)

Pectus carinatum (HP:0000768)

Pectus excavatum (HP:0000767)

Prominent sternum (HP:0000884)

Rachitic rosary (HP:0000897)

Sternal punctate calcifications (HP:0006637)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100892	HP:0100892	Abnormality of the xiphoid process	0	CL E G H
HP:0100892	HP:0100894	Broad xiphoid process	1	CL E G H
HP:0100892	HP:0100893	Prominent xiphoid process	1	CL E G H
HP:0100892	HP:0100891	Bifid xiphoid process	1	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.