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:
Inflammatory abnormality of the skin (HP:0011123)

Parent Node:
Neutrophilic infiltration of the skin (HP:0031234)

..Starting node
..Predominantly epidermal neutrophilic infiltrate (HP:0031235)

Term ID:

31235

Name:

Predominantly epidermal neutrophilic infiltrate

Synonym:

Definition:

Collection of neutrophils in the epidermis.

Comments:

Reference:

HP:0031235

Genes and Diseases:

Child Nodes:

Sister Nodes:

Predominantly dermal neutrophilic infiltrate (HP:0031236)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031235	HP:0031235	Predominantly epidermal neutrophilic infiltrate	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.