Human Phenotype Ontology 
Grandparent Node:
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Abnormality of skin physiology (HP:0011122)help
Grandparent Node:
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Increased inflammatory response (HP:0012649)help
Parent Node:
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Inflammatory abnormality of the skin (HP:0011123)help
..Starting node
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Erysipelas (HP:0001055)help
Term ID: 1055
Name: Erysipelas
Synonym: St. Anthony's Fire
Definition: Increased susceptibility to erysipelas, as manifested by a medical history of repeated episodes of erysipelas, which is a superficial infection of the skin, typically involving the lymphatic system.
Comments:
Reference: HP:0001055
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcne (HP:0001061) help
..expandAtopic dermatitis (HP:0001047) help
..expandCrusting erythematous dermatitis (HP:0007473) help
..expandCutaneous abscess (HP:0031292) help
..expandDeep dermal perivascular inflammatory infiltrate (HP:0031191) help
..expandEczema (HP:0000964) help
..expandErythema nodosum (HP:0012219) help
..expandErythroderma (HP:0001019) help
..expandFolliculitis (HP:0025084) help
..expandNeutrophilic infiltration of the skin (HP:0031234) help
..expandPerifolliculitis (HP:0012322) help
..expandPsoriasiform dermatitis (HP:0003765) help
..expandPustule (HP:0200039) help
..expandRecurrent skin infections (HP:0001581) help
..expandSkin rash (HP:0000988) help
..expandSuperficial dermal perivascular inflammatory infiltrate (HP:0031190) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001055HP:0001055Erysipelas0ADAMTS3 CL E G H9508219ORPHA:2136Hennekam syndromeHP:0040282 - Frequent1
HP:0001055HP:0001055Erysipelas0CCBE1 CL E G H14737229426OMIM:235510Hennekam lymphangiectasia-lymphedema syndrome.147
HP:0001055HP:0001055Erysipelas0CCBE1 CL E G H14737229426ORPHA:2136Hennekam syndromeHP:0040282 - Frequent147
HP:0001055HP:0001055Erysipelas0FAM111B CL E G H37439324200OMIM:615704Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosisHP:0040283 - Occasional6
HP:0001055HP:0001055Erysipelas0FAT4 CL E G H7963323109ORPHA:2136Hennekam syndromeHP:0040282 - Frequent114
HP:0001055HP:0001055Erysipelas0FLT4 CL E G H23243767ORPHA:79452Milroy diseaseHP:0040284 - Very rare90
HP:0001055HP:0001055Erysipelas0GJC2 CL E G H5716517494ORPHA:79452Milroy diseaseHP:0040284 - Very rare37
HP:0001055HP:0001055Erysipelas0KIF11 CL E G H38326388ORPHA:2526Microcephaly-lymphedema-chorioretinopathy syndromeHP:0040283 - Occasional46
HP:0001055HP:0001055Erysipelas0MEFV CL E G H42106998ORPHA:342Familial Mediterranean feverHP:0040282 - Frequent281
HP:0001055HP:0001055Erysipelas0MEFV CL E G H42106998OMIM:249100Familial Mediterranean fever, AR281
HP:0001055HP:0001055Erysipelas0MEFV CL E G H42106998OMIM:134610FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT281
HP:0001055HP:0001055Erysipelas0TNFRSF1A CL E G H713211916OMIM:142680Periodic fever, familial, autosomal dominant131
HP:0001055HP:0001055Erysipelas0TNFRSF1A CL E G H713211916ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndromeHP:0040281 - Very frequent131


Genes (9) :ADAMTS3 CCBE1 FAM111B FAT4 FLT4 GJC2 KIF11 MEFV TNFRSF1A

Diseases (10) :ORPHA:2136 OMIM:235510 OMIM:615704 ORPHA:79452 ORPHA:2526 ORPHA:342 OMIM:249100 OMIM:134610 OMIM:142680 ORPHA:32960
 

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