Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 anterior chamber morphology (HP:0000593)

Parent Node:
Anterior chamber flare (HP:0031616)

..Starting node
..Anterior chamber flare grade 1+ (HP:0031618)

Term ID:

31618

Name:

Anterior chamber flare grade 1+

Synonym:

Definition:

Faint anterior chamber flare.

Comments:

Reference:

HP:0031618

Genes and Diseases:

Child Nodes:

Sister Nodes:

Anterior chamber flare grade 2+ (HP:0031619)

Anterior chamber flare grade 3+ (HP:0031620)

Anterior chamber flare grade 4+ (HP:0031621)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031618	HP:0031618	Anterior chamber flare grade 1+	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.