Human Phenotype Ontology 
Grandparent Node:
expandAbnormal eyelid morphology (HP:0000492)help
Grandparent Node:
expandAbnormal hair morphology (HP:0001595)help
Parent Node:
expandAbnormal eyelash morphology (HP:0000499)help
..Starting node
..expandAbnormality of upper eyelashes (HP:0040051)help
Term ID: 40051
Name: Abnormality of upper eyelashes
Synonym: Abnormality of upper eyelashes
Definition:
Comments:
Reference: HP:0040051
Genes and Diseases:
 
       Child Nodes:
........expandLong upper eyelashes (HP:0007840) help
........expandSparse upper eyelashes (HP:0040050) help
........expandShort upper eyelashes (HP:0040054) help

 Sister Nodes: 
..expandAbnormality of lower eyelashes (HP:0040052) help
..expandCurly eyelashes (HP:0007665) help
..expandEctopic cilia of eyelid (HP:0430006) help
..expandLong eyelashes (HP:0000527) help
..expandLoss of eyelashes (HP:0011457) help
..expandMultiple rows of eyelashes (HP:0008496) help
..expandProminent eyelashes (HP:0011231) help
..expandShort eyelashes (HP:0010764) help
..expandSparse or absent eyelashes (HP:0200102) help
..expandTrichiasis (HP:0001128) help
..expandWhite eyelashes (HP:0002227) 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:0040051HP:0040051Abnormality of upper eyelashes0 CL E G H
HP:0040051HP:0040054Short upper eyelashes1 CL E G H
HP:0040051HP:0040050Sparse upper eyelashes1 CL E G H
HP:0040051HP:0007840Long upper eyelashes1 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.