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 skin physiology (HP:0011122)

Grandparent Node:
Increased inflammatory response (HP:0012649)

Parent Node:
Inflammatory abnormality of the skin (HP:0011123)

..Starting node
..Superficial dermal perivascular inflammatory infiltrate (HP:0031190)

Term ID:

31190

Name:

Superficial dermal perivascular inflammatory infiltrate

Synonym:

Superficial perivascular inflammatory infiltrate

Definition:

Numerous lymphocytes surrounding blood vessels in the superfical part of the dermis.

Comments:

Reference:

HP:0031190

Genes and Diseases:

Child Nodes:

Sister Nodes:

Acne (HP:0001061)

Atopic dermatitis (HP:0001047)

Crusting erythematous dermatitis (HP:0007473)

Cutaneous abscess (HP:0031292)

Deep dermal perivascular inflammatory infiltrate (HP:0031191)

Eczema (HP:0000964)

Erysipelas (HP:0001055)

Erythema nodosum (HP:0012219)

Erythroderma (HP:0001019)

Folliculitis (HP:0025084)

Neutrophilic infiltration of the skin (HP:0031234)

Perifolliculitis (HP:0012322)

Psoriasiform dermatitis (HP:0003765)

Pustule (HP:0200039)

Recurrent skin infections (HP:0001581)

Skin rash (HP:0000988)

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:0031190	HP:0031190	Superficial dermal perivascular inflammatory infiltrate	0	LDHA CL E G H	3939	6535	ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency	HP:0040283 - Occasional	35
HP:0031190	HP:0031190	Superficial dermal perivascular inflammatory infiltrate	0	SLURP1 CL E G H	57152	18746	ORPHA:87503	Mal de Meleda		15
HP:0031190	HP:0031190	Superficial dermal perivascular inflammatory infiltrate	0	TRPM4 CL E G H	54795	17993	OMIM:618531	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6; EKVP6		124

Genes (3) :LDHA SLURP1 TRPM4

Diseases (3) :ORPHA:284426 ORPHA:87503 OMIM:618531

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