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:
Embryonal neoplasm (HP:0002898)

Grandparent Node:
Germ cell neoplasia (HP:0100728)

Parent Node:
Teratoma (HP:0009792)

..Starting node
..Craniofacial teratoma (HP:0030755)

Term ID:

30755

Name:

Craniofacial teratoma

Synonym:

Definition:

A teratoma located in the craniofacial region.

Comments:

Reference:

HP:0030755

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cardiac teratoma (HP:0011674)

Epignathus (HP:0030767)

Mediastinal teratoma (HP:0030741)

Nasopharyngeal teratoma (HP:0031227)

Ovarian teratoma (HP:0012226)

Sacrococcygeal teratoma (HP:0030736)

Testicular teratoma (HP:0100616)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030755	HP:0030755	Craniofacial teratoma	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.