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
..expandBrow ptosis (HP:0031623)help
Term ID: 31623
Name: Brow ptosis
Synonym: Drooping brow
Definition: Drooping of the upper eyebrow below the superior orbital rim.
Comments:
Reference: HP:0031623
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal location of the eyebrow (HP:0040296) help
..expandAplasia/Hypoplasia of the eyebrow (HP:0100840) help
..expandBroad eyebrow (HP:0011229) 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:0031623HP:0031623Brow ptosis0 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.