Human Phenotype Ontology 
Grandparent Node:
expandAbnormal hair morphology (HP:0001595)help
Grandparent Node:
expandAbnormal ocular adnexa morphology (HP:0030669)help
Grandparent Node:
expandAbnormality of the periorbital region (HP:0000606)help
Parent Node:
expandAbnormal eyebrow morphology (HP:0000534)help
..Starting node
..expandAbnormal location of the eyebrow (HP:0040296)help
Term ID: 40296
Name: Abnormal location of the eyebrow
Synonym: Abnormal location of eyebrows; Abnormally placed eyebrows
Definition: Anomalous anatomical placement of the eyebrow.
Comments:
Reference: HP:0040296
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia of the eyebrow (HP:0100840) help
..expandBroad eyebrow (HP:0011229) help
..expandBrow ptosis (HP:0031623) help
..expandDouble eyebrow (HP:0010730) help
..expandHighly arched eyebrow (HP:0002553) help
..expandHorizontal eyebrow (HP:0011228) help
..expandLaterally curved eyebrow (HP:0007733) help
..expandLaterally extended eyebrow (HP:0011230) help
..expandLong eyebrows (HP:0004523) help
..expandMedial flaring of the eyebrow (HP:0010747) help
..expandSynophrys (HP:0000664) help
..expandThick eyebrow (HP:0000574) help
..expandWhite eyebrow (HP:0002226) 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:0040296HP:0040296Abnormal location of the eyebrow0SYT1 CL E G H685711509ORPHA:522077Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndromeHP:0040283 - Occasional1


Genes (1) :SYT1

Diseases (1) :ORPHA:522077
 

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