Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

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 skin morphology (HP:0011121)

Parent Node:
Localized skin lesion (HP:0011355)

..Starting node
..Lichenoid skin lesion (HP:0031452)

Term ID:

31452

Name:

Lichenoid skin lesion

Synonym:

Definition:

Mutliple skin lesions resembling those characteristic of the disease lichen planus. These lesions are violaceous (reddish-purple), shiny, isolated, flat-topped papules and plaques.

Comments:

Reference:

HP:0031452

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal perifollicular morphology (HP:0031285)

Annular cutaneous lesion (HP:0025528)

Aplasia/Hypoplasia of the skin (HP:0008065)

Atypical scarring of skin (HP:0000987)

Cafe-au-lait spot (HP:0000957)

Capillary malformation (HP:0025104)

Comedo (HP:0025249)

Cutaneous cyst (HP:0025245)

Hypopigmented skin patches (HP:0001053)

Macule (HP:0012733)

Milia (HP:0001056)

Molluscoid pseudotumors (HP:0000993)

Nevus (HP:0003764)

Papule (HP:0200034)

Serpiginous cutaneous lesion (HP:0025527)

Skin dimple (HP:0010781)

Skin erosion (HP:0200041)

Skin fissure (HP:0031057)

Skin nodule (HP:0200036)

Skin pit (HP:0100276)

Skin plaque (HP:0200035)

Skin tags (HP:0010609)

Skin ulcer (HP:0200042)

Skin vesicle (HP:0200037)

Xanthomatosis (HP:0000991)

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:0031452	HP:0031452	Lichenoid skin lesion	0	INSR CL E G H	3643	6091	ORPHA:769	Rabson-Mendenhall syndrome	HP:0040282 - Frequent	229
HP:0031452	HP:0031452	Lichenoid skin lesion	0	SLURP1 CL E G H	57152	18746	ORPHA:87503	Mal de Meleda		15

Genes (2) :INSR SLURP1

Diseases (2) :ORPHA:769 ORPHA:87503

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

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