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:
Neuroendocrine neoplasm (HP:0100634)

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

Parent Node:
Paraganglioma (HP:0002668)

..Starting node
..Pulmonary paraglioma (HP:0100636)

Term ID:

100636

Name:

Pulmonary paraglioma

Synonym:

Definition:

A rare paranglioma of the lung, tumors that arise from extra-adrenal chromaffin cells.

Comments:

Reference:

HP:0100636

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chemodectoma (HP:0030074)

Paraganglioma of head and neck (HP:0002864)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100636	HP:0100636	Pulmonary paraglioma	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.