Human Phenotype Ontology 
Grandparent Node:
Abnormality of the lymphatic system (HP:0100763)help
Parent Node:
Abnormal tongue morphology (HP:0030809)help
Parent Node:
Abnormality of the tonsils (HP:0100765)help
..Starting node
Abnormality of lingual tonsil (HP:3000076)help
Term ID: 3000076
Name: Abnormality of lingual tonsil
Definition: An abnormality of a lingual tonsil.
Reference: HP:3000076
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal nasopharyngeal adenoid morphology (HP:3000033) help
..expandAbsent tonsils (HP:0030813) help
..expandEnlarged tonsils (HP:0030812) help
..expandOrange discolored tonsils (HP:0030814) help
..expandRecurrent tonsillitis (HP:0011110) 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:3000076HP:3000076Abnormality of lingual tonsil0 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.