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:
Neuroblastic tumor (HP:0004376)

Grandparent Node:
Peripheral primitive neuroectodermal neoplasm (HP:0030067)

Parent Node:
Neuroblastoma (HP:0003006)

..Starting node
..Olfactory esthesioneuroblastoma (HP:0030068)

Term ID:

30068

Name:

Olfactory esthesioneuroblastoma

Synonym:

Definition:

A malignant olfactory neuroblastoma arising from the olfactory epithelium of the superior nasal cavity and cribriform plate.

Comments:

Reference:

HP:0030068

Genes and Diseases:

Child Nodes:

Sister Nodes:

Congenital neuroblastoma (HP:0006742)

Ganglioneuroblastoma (HP:0006747)

Localized neuroblastoma (HP:0006768)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030068	HP:0030068	Olfactory esthesioneuroblastoma	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.