Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the ovary (HP:0000137)help
Grandparent Node:
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Gonadal neoplasm (HP:0010785)help
Parent Node:
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Germinoma (HP:0100620)help
Parent Node:
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Ovarian neoplasm (HP:0100615)help
..Starting node
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Dysgerminoma (HP:0100621)help
Term ID: 100621
Name: Dysgerminoma
Synonym:
Definition: The presence of a dysgerminoma, i.e., an undifferentiated germ cell tumor of the ovary.
Comments:
Reference: HP:0100621
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandOvarian carcinoma (HP:0025318) help
..expandOvarian fibroma (HP:0010618) help
..expandOvarian gonadoblastoma (HP:0000149) help
..expandOvarian papillary adenocarcinoma (HP:0006774) help
..expandOvarian teratoma (HP:0012226) help
..expandOvarian thecoma (HP:0030983) 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:0100621HP:0100621Dysgerminoma0AKT1 CL E G H207391OMIM:167000Ovarian cancer.54
HP:0100621HP:0100621Dysgerminoma0CDH1 CL E G H9991748OMIM:167000Ovarian cancer.1003
HP:0100621HP:0100621Dysgerminoma0CTNNB1 CL E G H14992514OMIM:167000Ovarian cancer.88
HP:0100621HP:0100621Dysgerminoma0DHH CL E G H508462865OMIM:23342046,xy sex reversal 721
HP:0100621HP:0100621Dysgerminoma0ERBB2 CL E G H20643430OMIM:167000Ovarian cancer.77
HP:0100621HP:0100621Dysgerminoma0FGFR2 CL E G H22633689OMIM:123500Crouzon syndrome.175
HP:0100621HP:0100621Dysgerminoma0MAP3K1 CL E G H42146848OMIM:61376246,xy sex reversal 6.13
HP:0100621HP:0100621Dysgerminoma0OPCML CL E G H49788143OMIM:167000Ovarian cancer.5
HP:0100621HP:0100621Dysgerminoma0PIK3CA CL E G H52908975OMIM:167000Ovarian cancer.162
HP:0100621HP:0100621Dysgerminoma0PRKN CL E G H50718607OMIM:167000Ovarian cancer.138


Genes (10) :AKT1 CDH1 CTNNB1 DHH ERBB2 FGFR2 MAP3K1 OPCML PIK3CA PRKN

Diseases (4) :OMIM:167000 OMIM:233420 OMIM:123500 OMIM:613762
 

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