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
..Fractured rib (HP:0041159)

Term ID:

41159

Name:

Fractured rib

Synonym:

bone rib

Definition:

A partial or complete breakage of the rib.

Comments:

Reference:

HP:0041159

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0041159	HP:0041159	Fractured rib	0	LBR CL E G H	3930	6518	OMIM:215140	Greenberg dysplasia	70

Genes (1) :LBR

Diseases (1) :OMIM:215140

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