Human Phenotype Ontology 
Grandparent Node:
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Abnormal endometrium morphology (HP:0030126)help
Grandparent Node:
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Abnormal female reproductive system physiology (HP:0030012)help
Parent Node:
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Abnormal uterine cervix morphology (HP:0012888)help
Parent Node:
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Endometriosis (HP:0030127)help
..Starting node
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Cervical endometriosis (HP:0012889)help
Term ID: 12889
Name: Cervical endometriosis
Synonym:
Definition: Abnormal growth of endometrial cells (which are normally limited to the uterus) within the cervix.
Comments:
Reference: HP:0012889
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012889HP:0012889Cervical endometriosis0 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.