Human Phenotype Ontology 
Grandparent Node:
Abnormality of the integument (HP:0001574)help
Parent Node:
Abnormality of skin adnexa physiology (HP:0025276)help
..Starting node
Ipsilateral lack of facial sweating (HP:0007451)help
Term ID: 7451
Name: Ipsilateral lack of facial sweating
Definition: Inability to sweat on the same side of the face that is affected by ptosis and miosis. This is a feature of Horner syndrome.
Reference: HP:0007451
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAnhidrosis (HP:0000970) help
..expandCold-induced sweating (HP:0025278) help
..expandGeneralized anhidrosis (HP:0007459) help
..expandGustatory sweating (HP:0025277) help
..expandHypohidrosis or hyperhidrosis (HP:0007550) 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:0007451HP:0007451Ipsilateral lack of facial sweating0 CL E G H

Genes (0) :

Diseases (0) :

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