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:
Involuntary movements (HP:0004305)

Parent Node:
Tremor (HP:0001337)

..Starting node
..Rubral tremor (HP:0030665)

Term ID:

30665

Name:

Rubral tremor

Synonym:

Holmes' tremor

Definition:

Rubral tremor is characterized by a slow coarse tremor at rest that is exacerbated by postural adjustments and by guided voluntary movements.

Comments:

Reference:

HP:0030665

Genes and Diseases:

Child Nodes:

Sister Nodes:

Action tremor (HP:0002345)

Resting tremor (HP:0002322)

Tremor by anatomical site (HP:0030188)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030665	HP:0030665	Rubral tremor	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.