Human Phenotype Ontology 
Grandparent Node:
Abnormality of the integument (HP:0001574)help
Parent Node:
Abnormality of skin adnexa physiology (HP:0025276)help
..Starting node
Generalized anhidrosis (HP:0007459)help
Term ID: 7459
Name: Generalized anhidrosis
Synonym: Generalised anhidrosis; Generalised anhydrosis; Generalised inability to sweat; Generalized anhydrosis; Generalized inability to sweat
Reference: HP:0007459
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAnhidrosis (HP:0000970) help
..expandCold-induced sweating (HP:0025278) help
..expandGustatory sweating (HP:0025277) help
..expandHypohidrosis or hyperhidrosis (HP:0007550) help
..expandIpsilateral lack of facial sweating (HP:0007451) 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:0007459HP:0007459Generalized anhidrosis0ITPR2 CL E G H37096181OMIM:106190Anhidrosis, isolated, with normal sweat glands.1

Genes (1) :ITPR2

Diseases (1) :OMIM:106190

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