Human Phenotype Ontology 
Grandparent Node:
expandEmbryonal neoplasm (HP:0002898)help
Grandparent Node:
expandRenal neoplasm (HP:0009726)help
Parent Node:
expandAbnormality of connective tissue (HP:0003549)help
Parent Node:
expandEmbryonal renal neoplasm (HP:0011794)help
..Starting node
..expandCongenital mesoblastic nephroma (HP:0100881)help
Term ID: 100881
Name: Congenital mesoblastic nephroma
Synonym:
Definition: Congenital mesoblastic nephroma is a type of kidney tumor that is usually found before birth by ultrasound or within the first 3 months of life. It contains fibroblastic cells (connective tissue cells), and may spread to the other kidney or to nearby tissue.
Comments:
Reference: HP:0100881
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNephroblastoma (HP:0002667) help
..expandNephroblastomatosis (HP:0008643) 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:0100881HP:0100881Congenital mesoblastic nephroma0 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.