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:
Abnormal eyelid morphology (HP:0000492)

Grandparent Node:
Skin nodule (HP:0200036)

Parent Node:
Epidermoid cyst (HP:0200040)

Parent Node:
Nodular changes affecting the eyelids (HP:0010732)

..Starting node
..Cyst of the eyelid (HP:0010604)

Term ID:

10604

Name:

Cyst of the eyelid

Synonym:

Cyst of the eyelid; Eyelid bump; Eyelid mass; Lesion of the eyelid

Definition:

Comments:

Reference:

HP:0010604

Genes and Diseases:

Child Nodes:

........

Chalazion (HP:0010605)

Sister Nodes:

Hordeolum (HP:0010606)

Xanthelasma (HP:0001114)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010604	HP:0010604	Cyst of the eyelid	0	CL E G H
HP:0010604	HP:0010605	Chalazion	1	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.