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:
Neoplasm of the central nervous system (HP:0100006)

Parent Node:
Benign neoplasm of the central nervous system (HP:0100835)

Parent Node:
Germinoma (HP:0100620)

Parent Node:
Malignant neoplasm of the central nervous system (HP:0100836)

..Starting node
..Cerebral germinoma (HP:0100312)

Term ID:

100312

Name:

Cerebral germinoma

Synonym:

Definition:

The presence of a germ cell tumor of the cerebrum.

Comments:

Reference:

HP:0100312

Genes and Diseases:

Child Nodes:

Sister Nodes:

Choroid plexus carcinoma (HP:0030392)

Glioma (HP:0009733)

Medulloblastoma (HP:0002885)

Neuroblastic tumor (HP:0004376)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100312	HP:0100312	Cerebral germinoma	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.