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:
Epidermal thickening (HP:0011368)

Parent Node:
Ichthyosis (HP:0008064)

..Starting node
..Postnatal-onset ichthyosiform erythroderma (HP:0007395)

Term ID:

7395

Name:

Postnatal-onset ichthyosiform erythroderma

Synonym:

Postnatal-onset ichthyosis

Definition:

A type of ichthyosiform erythroderma with postnatal onset.

Comments:

Reference:

HP:0007395

Genes and Diseases:

Child Nodes:

Sister Nodes:

Congenital ichthyosiform erythroderma (HP:0007431)

Generalized ichthyosis (HP:0007503)

Ichthyosis follicularis (HP:0031291)

Localized epidermolytic hyperkeratosis (HP:0007559)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007395	HP:0007395	Postnatal-onset ichthyosiform erythroderma	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.