Human Phenotype Ontology 
Grandparent Node:
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Abnormal autonomic nervous system physiology (HP:0012332)help
Grandparent Node:
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Miosis (HP:0000616)help
Grandparent Node:
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Ptosis (HP:0000508)help
Parent Node:
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Horner syndrome (HP:0002277)help
..Starting node
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Congenital Horner syndrome (HP:0006837)help
Term ID: 6837
Name: Congenital Horner syndrome
Synonym:
Definition: A type of Horner syndrome with congenital onset.
Comments:
Reference: HP:0006837
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
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:0006837HP:0006837Congenital Horner syndrome0 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.