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 appendicular skeleton morphology (HP:0011844)

Grandparent Node:
Abnormal thorax morphology (HP:0000765)

Parent Node:
Abnormal shoulder morphology (HP:0003043)

..Starting node
..Shoulder impingement (HP:0030881)

Term ID:

30881

Name:

Shoulder impingement

Synonym:

Definition:

Trapping and compression of the rotator cuff tendons during shoulder movements.

Comments:

Reference:

HP:0030881

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of the glenoid fossa (HP:0011912)

Down-sloping shoulders (HP:0200021)

Internally rotated shoulders (HP:0006659)

Limited shoulder movement (HP:0006467)

Scapulohumeral synostosis (HP:0006595)

Shoulder dislocation (HP:0003834)

Shoulder flexion contracture (HP:0003044)

Stiff shoulders (HP:0009742)

Stippled calcification of the shoulder (HP:0003836)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030881	HP:0030881	Shoulder impingement	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.