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

..Starting node
..Fracture type (HP:4000042)

Term ID:

4000042

Name:

Fracture type

Synonym:

Definition:

Category of fracture. Terms from this subontology can be used together with terms in the subontology that descends from Bone fracture (HP:0020110).

Comments:

Reference:

HP:4000042

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:4000042	HP:4000042	Fracture type	0	CL E G H
HP:4000042	HP:4000047	Compression fracture	1	CL E G H
HP:4000042	HP:4000053	Displaced fracture	1	CL E G H
HP:4000042	HP:4000046	Oblique fracture	1	CL E G H
HP:4000042	HP:4000052	Avulsion fracture	1	CL E G H
HP:4000042	HP:4000045	Spiral fracture	1	CL E G H
HP:4000042	HP:4000051	Closed fracture	1	CL E G H
HP:4000042	HP:4000044	Transverse fracture	1	CL E G H
HP:4000042	HP:4000050	Open fracture	1	CL E G H
HP:4000042	HP:4000043	Greenstick fracture	1	CL E G H
HP:4000042	HP:4000049	Segmental fracture	1	CL E G H
HP:4000042	HP:4000048	Comminuted fracture	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.