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:
Neuroectodermal neoplasm (HP:0030061)

Parent Node:
Neuroepithelial neoplasm (HP:0030063)

..Starting node
..Neurocytoma (HP:0030064)

Term ID:

30064

Name:

Neurocytoma

Synonym:

Definition:

A benign brain tumor composed of neural elements which most often arise from the septum pellucidum and the walls of the lateral ventricles.

Comments:

Reference:

HP:0030064

Genes and Diseases:

Child Nodes:

Sister Nodes:

Glioma (HP:0009733)

Pinealoma (HP:0010799)

Primitive neuroectodermal tumor (HP:0030065)

Retinoblastoma (HP:0009919)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030064	HP:0030064	Neurocytoma	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.