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:
Vocal cord paralysis (HP:0001605)

Parent Node:
Vocal cord paresis (HP:0001604)

..Starting node
..Unilateral vocal cord paresis (HP:0012821)

Term ID:

12821

Name:

Unilateral vocal cord paresis

Synonym:

Definition:

Decreased strength of the vocal fold on one side.

Comments:

Reference:

HP:0012821

Genes and Diseases:

Child Nodes:

Sister Nodes:

Bilateral vocal cord paresis (HP:0012822)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012821	HP:0012821	Unilateral vocal cord paresis	0	HAAO CL E G H	23498	4796	OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1	2

Genes (1) :HAAO

Diseases (1) :OMIM:617660

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.