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:
Abnormal lung morphology (HP:0002088)

Grandparent Node:
Neoplasm of the respiratory system (HP:0100606)

Parent Node:
Abnormal bronchus morphology (HP:0025426)

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

..Starting node
..Bronchial neoplasm (HP:0030077)

Term ID:

30077

Name:

Bronchial neoplasm

Synonym:

Definition:

A tumor originating in a bronchus.

Comments:

Reference:

HP:0030077

Genes and Diseases:

Child Nodes:

Sister Nodes:

Lung fibroma (HP:0010616)

Neoplasm of the tracheobronchial system (HP:0100552)

Non-small cell lung carcinoma (HP:0030358)

Pulmonary chondroma (HP:0031474)

Pulmonary lymphangiomyomatosis (HP:0012798)

Pulmonary lymphoma (HP:0011953)

Pulmonary paraglioma (HP:0100636)

Small cell lung carcinoma (HP:0030357)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030077	HP:0030077	Bronchial neoplasm	0	CL E G H
HP:0030077	HP:0033002	Bronchial 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.