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)

Parent Node:
Abnormal tracheal morphology (HP:0002778)

..Starting node
..Tracheomegaly (HP:0010778)

Term ID:

10778

Name:

Tracheomegaly

Synonym:

Definition:

Marked widening of the trachea.

Comments:

Reference:

HP:0010778

Genes and Diseases:

Child Nodes:

........

Tracheobronchmegaly (HP:0010776)

Sister Nodes:

Anomalous tracheal cartilage (HP:0004468)

Diverticulosis of trachea (HP:0006509)

Neoplasm of the trachea (HP:0100551)

Tracheal calcification (HP:0002787)

Tracheal cartilaginous sleeve (HP:0005347)

Tracheal stenosis (HP:0002777)

Tracheoesophageal fistula (HP:0002575)

Tracheomalacia (HP:0002779)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010778	HP:0010778	Tracheomegaly	0	CL E G H
HP:0010778	HP:0010776	Tracheobronchmegaly	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.