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 bone ossification (HP:0011849)

Parent Node:
Ectopic ossification (HP:0011986)

..Starting node
..Soft-tissue ossification around the shoulders (HP:0003837)

Term ID:

3837

Name:

Soft-tissue ossification around the shoulders

Synonym:

Calcification of the soft-tissue around the shoulders

Definition:

Formation of calcified tissue in the soft tissues surrounding the shoulder.

Comments:

Reference:

HP:0003837

Genes and Diseases:

Child Nodes:

Sister Nodes:

Ectopic ossification in ligament tissue (HP:0011989)

Ectopic ossification in muscle tissue (HP:0011987)

Ectopic ossification in tendon tissue (HP:0011988)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003837	HP:0003837	Soft-tissue ossification around the shoulders	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.