Human Phenotype Ontology 
Grandparent Node:
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Abnormal uterus morphology (HP:0031105)help
Grandparent Node:
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Genital neoplasm (HP:0010787)help
Parent Node:
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Abnormal uterine cervix morphology (HP:0012888)help
Parent Node:
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Uterine neoplasm (HP:0010784)help
..Starting node
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Cervix cancer (HP:0030079)help
Term ID: 30079
Name: Cervix cancer
Synonym:
Definition: A tumor of the uterine cervix.
Comments:
Reference: HP:0030079
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEndometrial carcinoma (HP:0012114) help
..expandUterine leiomyoma (HP:0000131) help
..expandUterine leiomyosarcoma (HP:0002891) 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:0030079HP:0030079Cervix cancer0CDKN1B CL E G H10271785ORPHA:276152Multiple endocrine neoplasia type 4HP:0040283 - Occasional102
HP:0030079HP:0030079Cervix cancer0CXCR4 CL E G H78522561ORPHA:51636WHIM syndromeHP:0040283 - Occasional9
HP:0030079HP:0030079Cervix cancer0SRY CL E G H673611311ORPHA:177245,X/46,XY mixed gonadal dysgenesisHP:0040283 - Occasional23
HP:0030079HP:0030079Cervix cancer0STK11 CL E G H679411389ORPHA:2869Peutz-Jeghers syndromeHP:0040283 - Occasional740


Genes (4) :CDKN1B CXCR4 SRY STK11

Diseases (4) :ORPHA:276152 ORPHA:51636 ORPHA:1772 ORPHA:2869
 

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