Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Constitutional symptom (HP:0025142)help
..Starting node
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Night sweats (HP:0030166)help
Term ID: 30166
Name: Night sweats
Synonym: Night sweats; Nocturnal hyperhidrosis
Definition: Occurrence of excessive sweating during sleep.
Comments:
Reference: HP:0030166
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAsthenia (HP:0025406) help
..expandBody odor (HP:0500001) help
..expandChest tightness (HP:0031352) help
..expandChills (HP:0025143) help
..expandFatigue (HP:0012378) help
..expandHot flashes (HP:0031217) help
..expandImpairment of activities of daily living (HP:0031058) help
..expandPain (HP:0012531) help
..expandShivering (HP:0025144) 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:0030166HP:0030166Night sweats0BCL2 CL E G H596990ORPHA:545Follicular lymphomaHP:0040281 - Very frequent1
HP:0030166HP:0030166Night sweats0BCL6 CL E G H6041001ORPHA:545Follicular lymphomaHP:0040281 - Very frequent1
HP:0030166HP:0030166Night sweats0GATA2 CL E G H26244171ORPHA:98827Unclassified myelodysplastic syndromeHP:0040283 - Occasional137
HP:0030166HP:0030166Night sweats0HLA-DRB1 CL E G H31234948ORPHA:545Follicular lymphomaHP:0040281 - Very frequent2
HP:0030166HP:0030166Night sweats0IFNGR1 CL E G H34595439OMIM:209950Immunodeficiency 27A, mycobacteriosis, AR60
HP:0030166HP:0030166Night sweats0IGH CL E G H34925477ORPHA:545Follicular lymphomaHP:0040281 - Very frequent7
HP:0030166HP:0030166Night sweats0JAG1 CL E G H1826188OMIM:619574CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH; CMT2HH257
HP:0030166HP:0030166Night sweats0NAB2 CL E G H46657627ORPHA:2126Solitary fibrous tumor/hemangiopericytomaHP:0040284 - Very rare
HP:0030166HP:0030166Night sweats0SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040282 - Frequent129
HP:0030166HP:0030166Night sweats0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040282 - Frequent82
HP:0030166HP:0030166Night sweats0STAT6 CL E G H677811368ORPHA:2126Solitary fibrous tumor/hemangiopericytomaHP:0040284 - Very rare1
HP:0030166HP:0030166Night sweats0TH CL E G H705411782ORPHA:101150Autosomal recessive dopa-responsive dystoniaHP:0040282 - Frequent80
HP:0030166HP:0030166Night sweats0TSPOAP1 CL E G H925616831ORPHA:101150Autosomal recessive dopa-responsive dystoniaHP:0040282 - Frequent2
HP:0030166HP:0030166Night sweats0UBA1 CL E G H731712469OMIM:301054VEXAS SYNDROME; VEXAS35


Genes (14) :BCL2 BCL6 GATA2 HLA-DRB1 IFNGR1 IGH JAG1 NAB2 SDHD SLC25A13 STAT6 TH TSPOAP1 UBA1

Diseases (9) :ORPHA:545 ORPHA:98827 OMIM:209950 OMIM:619574 ORPHA:2126 ORPHA:100093 ORPHA:247585 ORPHA:101150 OMIM:301054
 

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