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 tracheobronchial morphology (HP:0005607)

Grandparent Node:
Neoplasm of the lung (HP:0100526)

Parent Node:
Abnormal tracheal morphology (HP:0002778)

Parent Node:
Neoplasm of the tracheobronchial system (HP:0100552)

..Starting node
..Neoplasm of the trachea (HP:0100551)

Term ID:

100551

Name:

Neoplasm of the trachea

Synonym:

Tracheal neoplasm

Definition:

A neoplasm of the trachea.

Comments:

Reference:

HP:0100551

Genes and Diseases:

Child Nodes:

Sister Nodes:

Alveolar cell carcinoma (HP:0006519)

Pleuropulmonary blastoma (HP:0100528)

Tracheobronchial leiomyomatosis (HP:0006524)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100551	HP:0100551	Neoplasm of the trachea	0	CL E G H
HP:0100551	HP:0033003	Tracheal papilloma	1	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.