Human Phenotype Ontology 
Grandparent Node:
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Neoplasm by histology (HP:0011792)help
Parent Node:
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Hamartoma (HP:0010566)help
..Starting node
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Fibrous hamartoma (HP:0100882)help
Term ID: 100882
Name: Fibrous hamartoma
Synonym: Fibrous hamartoma of infancy
Definition: A rare, benign soft tissue tumor that typically occurs within the first two years of life.
Comments:
Reference: HP:0100882
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCerebral hamartoma (HP:0009731) help
..expandChorangioma (HP:0100883) help
..expandCutaneous hamartoma (HP:0031111) help
..expandHamartoma of the eye (HP:0010568) help
..expandHamartomatous polyposis (HP:0004390) help
..expandLymphangioma (HP:0100764) help
..expandNumerous nevi (HP:0001054) help
..expandOdontoma (HP:0011068) help
..expandRenal hamartoma (HP:0008696) 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:0100882HP:0100882Fibrous hamartoma0 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.