Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the integument (HP:0001574)help
Parent Node:
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Abnormality of skin adnexa physiology (HP:0025276)help
..Starting node
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Ipsilateral lack of facial sweating (HP:0007451)help
Term ID: 7451
Name: Ipsilateral lack of facial sweating
Synonym:
Definition:
Comments:
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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
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 August 2021 release.