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

..Starting node
..Fractured lumbar vertebra (HP:0041168)

Term ID:

41168

Name:

Fractured lumbar vertebra

Synonym:

bone lumbar vertebra

Definition:

A partial or complete breakage of the lumbar vertebra.

Comments:

Reference:

HP:0041168

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0041168	HP:0041168	Fractured lumbar vertebra	0	CL E G H
HP:0041168	HP:0041087	Compression-fractured lumbar vertebra	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.