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:
Abnormality of the curvature of the vertebral column (HP:0010674)

Parent Node:
Scoliosis (HP:0002650)

..Starting node
..Compensatory scoliosis (HP:0100884)

Term ID:

100884

Name:

Compensatory scoliosis

Synonym:

Definition:

A scoliosis which is the results of a difference in leg length (which might be due to hemihypertrophy or hemihypotrophy of a leg) and the resulting tilting of the pelvis. If untreated this will lead to the development of scoliosis over time.

Comments:

Reference:

HP:0100884

Genes and Diseases:

Child Nodes:

Sister Nodes:

Kyphoscoliosis (HP:0002751)

Progressive congenital scoliosis (HP:0008458)

Thoracic scoliosis (HP:0002943)

Thoracolumbar scoliosis (HP:0002944)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100884	HP:0100884	Compensatory scoliosis	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.

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