Human Phenotype Ontology 
Grandparent Node:
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Localized skin lesion (HP:0011355)help
Parent Node:
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Papule (HP:0200034)help
..Starting node
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Intermittent generalized erythematous papular rash (HP:0007432)help
Term ID: 7432
Name: Intermittent generalized erythematous papular rash
Synonym: Intermittent generalised erythematous papular rash
Definition:
Comments:
Reference: HP:0007432
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandErythematous papule (HP:0030350) help
..expandGottron's papules (HP:0025508) help
..expandHyperkeratotic papule (HP:0045059) help
..expandHyperpigmented papule (HP:0025473) help
..expandPiezogenic pedal papules (HP:0025509) help
..expandSkin-colored papule (HP:0025512) help
..expandVerrucous papule (HP:0012500) help
..expandWhite papule (HP:0031289) help
..expandYellow papule (HP:0025507) 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:0007432HP:0007432Intermittent generalized erythematous papular rash0LDHA CL E G H39396535ORPHA:284426Glycogen storage disease due to lactate dehydrogenase M-subunit deficiencyHP:0040283 - Occasional35
HP:0007432HP:0007432Intermittent generalized erythematous papular rash0NOD2 CL E G H641275331OMIM:186580Blau syndrome187


Genes (2) :LDHA NOD2

Diseases (2) :ORPHA:284426 OMIM:186580
 

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