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:
Immunologic hypersensitivity (HP:0100326)

Parent Node:
Anaphylactic shock (HP:0100845)

..Starting node
..Idiopathic anaphylaxis (HP:0410148)

Term ID:

410148

Name:

Idiopathic anaphylaxis

Synonym:

Definition:

A rare form of anaphylaxis for which triggers cannot be identified despite a detailed history and careful diagnostic assessment.

Comments:

Reference:

HP:0410148

Genes and Diseases:

Child Nodes:

Sister Nodes:

Drug-induced anaphylaxis (HP:0410149)

Exercise induced anaphylaxis (HP:0410139)

Food-induced anaphylaxis (HP:0500095)

Venom-induced anaphylaxis (HP:0500096)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410148	HP:0410148	Idiopathic anaphylaxis	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.