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:
Periorbital edema (HP:0100539)

Parent Node:
Palpebral edema (HP:0100540)

..Starting node
..Lower eyelid edema (HP:0012568)

Term ID:

12568

Name:

Lower eyelid edema

Synonym:

Cellulitis of lower eyelid; Fullness of lower eyelid; Lower eyelid oedema; Puffiness of lower eyelid; Swelling of lower eyelid

Definition:

Edema in the region of the Lower eyelid.

Comments:

Reference:

HP:0012568

Genes and Diseases:

Child Nodes:

Sister Nodes:

Blepharochalasis (HP:0010749)

Upper eyelid edema (HP:0012724)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012568	HP:0012568	Lower eyelid edema	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.