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 pelvic girdle bone morphology (HP:0002644)

Parent Node:
Abnormal pelvis bone morphology (HP:0040163)

..Starting node
..Pelvic bone asymmetry (HP:0010453)

Term ID:

10453

Name:

Pelvic bone asymmetry

Synonym:

Asymmetric pelvis; Pelvic asymmetry

Definition:

Pelvic asymmetry refers to asymmetric positioning of landmarks on the two sides of the pelvis and may have a structural or functional etiology.

Comments:

Reference:

HP:0010453

Genes and Diseases:

Child Nodes:

Sister Nodes:

Halberd-shaped pelvis (HP:0002826)

Large pelvis bone (HP:0010779)

Narrow pelvis bone (HP:0003275)

Pelvic bone exostoses (HP:0003276)

Square pelvis bone (HP:0003278)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010453	HP:0010453	Pelvic bone asymmetry	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.