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)

Parent Node:
Hooded eyelid (HP:0030820)

..Starting node
..Hooded lower eyelid (HP:0030821)

Term ID:

30821

Name:

Hooded lower eyelid

Synonym:

Definition:

Lower eyelid partly covered by skin when eyes are open.

Comments:

Reference:

HP:0030821

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hooded upper eyelid (HP:0030822)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030821	HP:0030821	Hooded lower eyelid	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.