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:
Impairment in personality functioning (HP:0031466)

Parent Node:
Abnormal fear/anxiety-related behavior (HP:0100852)

..Starting node
..Claustrophobia (HP:0025253)

Term ID:

25253

Name:

Claustrophobia

Synonym:

Definition:

An abnormal fear of being in a closed or narrow space with no escape.

Comments:

Reference:

HP:0025253

Genes and Diseases:

Child Nodes:

Sister Nodes:

Agoraphobia (HP:0000756)

Anxiety (HP:0000739)

Panic attack (HP:0025269)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025253	HP:0025253	Claustrophobia	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.