Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Neoplasm of the thyroid gland (HP:0100031)

Parent Node:
Thyroid adenoma (HP:0000854)

..Starting node
..Thyroid papillary adenoma (HP:0011777)

Term ID:

11777

Name:

Thyroid papillary adenoma

Synonym:

Definition:

Comments:

Reference:

HP:0011777

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hurthle cell thyroid adenoma (HP:0006781)

Thyroid atypical adenoma (HP:0011778)

Thyroid follicular adenoma (HP:0011774)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011777	HP:0011777	Thyroid papillary adenoma	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.