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:
Abnormal sacrum morphology (HP:0005107)

Grandparent Node:
Teratoma (HP:0009792)

Parent Node:
Sacrococcygeal teratoma (HP:0030736)

..Starting node
..Altman type II sacrococcygeal teratoma (HP:0030738)

Term ID:

30738

Name:

Altman type II sacrococcygeal teratoma

Synonym:

Definition:

A type of sacrococcygeal teratoma that is predominantly external but has a large intrapelvic component.

Comments:

Reference:

HP:0030738

Genes and Diseases:

Child Nodes:

Sister Nodes:

Altman type I sacrococcygeal teratoma (HP:0030737)

Altman type III sacrococcygeal teratoma (HP:0030739)

Presacral teratoma (HP:0009793)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030738	HP:0030738	Altman type II sacrococcygeal 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.