Human Phenotype Ontology 
Grandparent Node:
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Hypohidrosis or hyperhidrosis (HP:0007550)help
Parent Node:
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Hyperhidrosis (HP:0000975)help
..Starting node
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Episodic hyperhidrosis (HP:0001069)help
Term ID: 1069
Name: Episodic hyperhidrosis
Synonym: Hyperhidrosis, episodic; Sporadic excessive sweating
Definition: Intermittent episodes of abnormally increased perspiration.
Comments:
Reference: HP:0001069
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPalmar hyperhidrosis (HP:0006089) 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:0001069HP:0001069Episodic hyperhidrosis0ABCC8 CL E G H683359ORPHA:276575Autosomal dominant hyperinsulinism due to SUR1 deficiencyHP:0040282 - Frequent245
HP:0001069HP:0001069Episodic hyperhidrosis0ALDOB CL E G H229417ORPHA:469Hereditary fructose intoleranceHP:0040283 - Occasional73
HP:0001069HP:0001069Episodic hyperhidrosis0DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent
HP:0001069HP:0001069Episodic hyperhidrosis0DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent44
HP:0001069HP:0001069Episodic hyperhidrosis0ELP1 CL E G H85185959OMIM:223900Neuropathy, hereditary sensory and autonomic, type III.133
HP:0001069HP:0001069Episodic hyperhidrosis0EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent112
HP:0001069HP:0001069Episodic hyperhidrosis0FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent301
HP:0001069HP:0001069Episodic hyperhidrosis0HNF1A CL E G H692711621ORPHA:324575Hyperinsulinism due to HNF1A deficiencyHP:0040282 - Frequent161
HP:0001069HP:0001069Episodic hyperhidrosis0KCNJ11 CL E G H37676257ORPHA:276580Autosomal dominant hyperinsulinism due to Kir6.2 deficiencyHP:0040282 - Frequent127
HP:0001069HP:0001069Episodic hyperhidrosis0KIF1A CL E G H547888OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.276
HP:0001069HP:0001069Episodic hyperhidrosis0KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent202
HP:0001069HP:0001069Episodic hyperhidrosis0MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent84
HP:0001069HP:0001069Episodic hyperhidrosis0MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent4
HP:0001069HP:0001069Episodic hyperhidrosis0NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent1952
HP:0001069HP:0001069Episodic hyperhidrosis0RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent572
HP:0001069HP:0001069Episodic hyperhidrosis0RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent572
HP:0001069HP:0001069Episodic hyperhidrosis0RETREG1 CL E G H5446325964OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.54
HP:0001069HP:0001069Episodic hyperhidrosis0RETREG1 CL E G H5446325964OMIM:613115Neuropathy, hereditary sensory and autonomic, type IIB.54
HP:0001069HP:0001069Episodic hyperhidrosis0SCN9A CL E G H633510597OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.318
HP:0001069HP:0001069Episodic hyperhidrosis0SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent304
HP:0001069HP:0001069Episodic hyperhidrosis0SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent55
HP:0001069HP:0001069Episodic hyperhidrosis0SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent237
HP:0001069HP:0001069Episodic hyperhidrosis0SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent237
HP:0001069HP:0001069Episodic hyperhidrosis0SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent147
HP:0001069HP:0001069Episodic hyperhidrosis0SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent129
HP:0001069HP:0001069Episodic hyperhidrosis0SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent129
HP:0001069HP:0001069Episodic hyperhidrosis0SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent
HP:0001069HP:0001069Episodic hyperhidrosis0TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent131
HP:0001069HP:0001069Episodic hyperhidrosis0UCP2 CL E G H735112518ORPHA:276556Hyperinsulinism due to UCP2 deficiencyHP:0040282 - Frequent15
HP:0001069HP:0001069Episodic hyperhidrosis0VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent490
HP:0001069HP:0001069Episodic hyperhidrosis0VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent490
HP:0001069HP:0001069Episodic hyperhidrosis0WNK1 CL E G H6512514540OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.199


Genes (27) :ABCC8 ALDOB DLST DNMT3A ELP1 EPAS1 FH HNF1A KCNJ11 KIF1A KIF1B MAX MDH2 NF1 RET RETREG1 SCN9A SDHA SDHAF2 SDHB SDHC SDHD SLC25A11 TMEM127 UCP2 VHL WNK1

Diseases (10) :ORPHA:276575 ORPHA:469 ORPHA:29072 ORPHA:276621 OMIM:223900 ORPHA:324575 ORPHA:276580 OMIM:201300 OMIM:613115 ORPHA:276556
 

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