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 visual fixation (HP:0025404)

Parent Node:
Eccentric visual fixation (HP:0025549)

..Starting node
..Absolute eccentric fixation (HP:0500072)

Term ID:

500072

Name:

Absolute eccentric fixation

Synonym:

Definition:

Eccentric fixation in which the angle of eccentricity equals the objective angle of deviation.

Comments:

Reference:

HP:0500072

Genes and Diseases:

Child Nodes:

Sister Nodes:

Parafoveal fixation (HP:0031768)

Peripheral fixation (HP:0031769)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500072	HP:0500072	Absolute eccentric fixation	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.