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:
Abnormality of the head (HP:0000234)

Parent Node:
Abnormal scalp morphology (HP:0001965)

..Starting node
..Scalp tenderness (HP:0100809)

Term ID:

100809

Name:

Scalp tenderness

Synonym:

Allodynia of scalp; Scalp hypersensitivity; Scalp pain; Scalp tenderness

Definition:

Pain or discomfort of the scalp elicited by palpation.

Comments:

Reference:

HP:0100809

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of the scalp hair (HP:0100037)

Cutis gyrata of scalp (HP:0010541)

Prominent scalp veins (HP:0001043)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100809	HP:0100809	Scalp tenderness	0	ALX4 CL E G H	60529	450	ORPHA:60015	Enlarged parietal foramina	HP:0040283 - Occasional	132
HP:0100809	HP:0100809	Scalp tenderness	0	MSX2 CL E G H	4488	7392	ORPHA:60015	Enlarged parietal foramina	HP:0040283 - Occasional	45

Genes (2) :ALX4 MSX2

Diseases (1) :ORPHA:60015

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.