Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of the lymphatic system (HP:0100763)

Parent Node:
Abnormal tongue morphology (HP:0030809)

Parent Node:
Abnormality of the tonsils (HP:0100765)

..Starting node
..Abnormality of lingual tonsil (HP:3000076)

Term ID:

3000076

Name:

Abnormality of lingual tonsil

Synonym:

Definition:

An abnormality of a lingual tonsil.

Comments:

Reference:

HP:3000076

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal nasopharyngeal adenoid morphology (HP:3000033)

Absent tonsils (HP:0030813)

Enlarged tonsils (HP:0030812)

Orange discolored tonsils (HP:0030814)

Recurrent tonsillitis (HP:0011110)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:3000076	HP:3000076	Abnormality of lingual tonsil	0	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.