Human Phenotype Ontology 
Grandparent Node:
expand
Sparse hair (HP:0008070)help
Grandparent Node:
expand
Sparse or absent eyelashes (HP:0200102)help
Parent Node:
expand
Abnormality of upper eyelashes (HP:0040051)help
Parent Node:
expand
Sparse eyelashes (HP:0000653)help
..Starting node
..expand
Sparse upper eyelashes (HP:0040050)help
Term ID: 40050
Name: Sparse upper eyelashes
Synonym: Hypotrichosis of upper eyelashes; Partial absence of upper eyelashes; Sparse upper eyelashes
Definition:
Comments:
Reference: HP:0040050
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandSparse lower eyelashes (HP:0007776) 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:0040050HP:0040050Sparse upper eyelashes0 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.