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:
Goiter (HP:0000853)

Parent Node:
Nodular goiter (HP:0005994)

..Starting node
..Uninodular goiter (HP:0011773)

Term ID:

11773

Name:

Uninodular goiter

Synonym:

Uninodular goitre

Definition:

Enlargement of the thyroid gland related to a singular nodule in the thyroid gland.

Comments:

Reference:

HP:0011773

Genes and Diseases:

Child Nodes:

Sister Nodes:

Multinodular goiter (HP:0005987)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011773	HP:0011773	Uninodular goiter	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.