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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006837HP:0006837Congenital Horner syndrome0COL25A1 CL E G H8457018603ORPHA:91411Congenital ptosis3
HP:0006837HP:0006837Congenital Horner syndrome0GNB2 CL E G H27834398OMIM:619503NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF
HP:0006837HP:0006837Congenital Horner syndrome0ZFHX4 CL E G H7977630939ORPHA:91411Congenital ptosis


Genes (3) :COL25A1 GNB2 ZFHX4

Diseases (2) :ORPHA:91411 OMIM:619503
 

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