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:
Abnormal nervous system physiology (HP:0012638)

Parent Node:
Headache (HP:0002315)

..Starting node
..Thunderclap headache (HP:0030907)

Term ID:

30907

Name:

Thunderclap headache

Synonym:

Definition:

Severe head pain with sudden onset, reaching its maximum intensity in less than one minute and lasting from one hour to ten days.

Comments:

Reference:

HP:0030907

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cluster headache (HP:0012199)

Hypnic headache (HP:0012459)

Migraine (HP:0002076)

Occipital neuralgia (HP:0012318)

Recurrent paroxysmal headache (HP:0002331)

Tension-type headache (HP:0012228)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030907	HP:0030907	Thunderclap headache	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.