Human Phenotype Ontology 
Grandparent Node:
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Embryonal neoplasm (HP:0002898)help
Grandparent Node:
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Germ cell neoplasia (HP:0100728)help
Parent Node:
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Abnormal sacrum morphology (HP:0005107)help
Parent Node:
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Teratoma (HP:0009792)help
..Starting node
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Sacrococcygeal teratoma (HP:0030736)help
Term ID: 30736
Name: Sacrococcygeal teratoma
Synonym:
Definition: A teratoma arising in the sacro-coccygeal region.
Comments:
Reference: HP:0030736
Genes and Diseases:
 
       Child Nodes:
........expandPresacral teratoma (HP:0009793) help
........expandAltman type I sacrococcygeal teratoma (HP:0030737) help
........expandAltman type II sacrococcygeal teratoma (HP:0030738) help
........expandAltman type III sacrococcygeal teratoma (HP:0030739) help

 Sister Nodes: 
..expandCardiac teratoma (HP:0011674) help
..expandCraniofacial teratoma (HP:0030755) help
..expandEpignathus (HP:0030767) help
..expandMediastinal teratoma (HP:0030741) help
..expandNasopharyngeal teratoma (HP:0031227) help
..expandOvarian teratoma (HP:0012226) help
..expandTesticular teratoma (HP:0100616) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030736HP:0030736Sacrococcygeal teratoma0APC2 CL E G H1029724036ORPHA:821Sotos syndromeHP:0040284 - Very rare1
HP:0030736HP:0030736Sacrococcygeal teratoma0MNX1 CL E G H31104979ORPHA:1552Currarino syndromeHP:0040281 - Very frequent17
HP:0030736HP:0030736Sacrococcygeal teratoma0MNX1 CL E G H31104979OMIM:176450Currarino syndrome17
HP:0030736HP:0030736Sacrococcygeal teratoma0NSD1 CL E G H6432414234ORPHA:821Sotos syndromeHP:0040284 - Very rare544
HP:0030736HP:0030736Sacrococcygeal teratoma0SETBP1 CL E G H2604015573OMIM:269150Schinzel-Giedion midface-retraction syndrome.143
HP:0030736HP:0030736Sacrococcygeal teratoma0SETBP1 CL E G H2604015573ORPHA:798Schinzel-Giedion syndromeHP:0040284 - Very rare143
HP:0030736HP:0030736Sacrococcygeal teratoma0SETD2 CL E G H2907218420ORPHA:821Sotos syndromeHP:0040284 - Very rare60
HP:0030736HP:0030739Altman type III sacrococcygeal teratoma1 CL E G H
HP:0030736HP:0030738Altman type II sacrococcygeal teratoma1 CL E G H
HP:0030736HP:0030737Altman type I sacrococcygeal teratoma1 CL E G H
HP:0030736HP:0009793Presacral teratoma1MNX1 CL E G H31104979OMIM:176450Currarino syndrome.17


Genes (5) :APC2 MNX1 NSD1 SETBP1 SETD2

Diseases (5) :ORPHA:821 ORPHA:1552 OMIM:176450 OMIM:269150 ORPHA:798
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.