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:
Localized skin lesion (HP:0011355)

Parent Node:
Xanthomatosis (HP:0000991)

..Starting node
..Verruciform xanthoma (HP:0031517)

Term ID:

31517

Name:

Verruciform xanthoma

Synonym:

Definition:

A papillary or cauliflower-like growth characterized by the presence of foamy histiocytes within the elongated dermal papillae forms.

Comments:

Reference:

HP:0031517

Genes and Diseases:

Child Nodes:

Sister Nodes:

Atheroeruptive xanthoma (HP:0001039)

Eruptive xanthomas (HP:0001013)

Tendon xanthomatosis (HP:0010874)

Tuberous xanthoma (HP:0031290)

Xanthelasma (HP:0001114)

Xanthomas of the palmar creases (HP:0025530)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031517	HP:0031517	Verruciform xanthoma	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.