Human Phenotype Ontology 
Grandparent Node:
expandAbsent facial hair (HP:0002550)help
Grandparent Node:
expandSparse or absent eyelashes (HP:0200102)help
Parent Node:
expandAbsent eyelashes (HP:0000561)help
..Starting node
..expandAbsent lower eyelashes (HP:0007646)help
Term ID: 7646
Name: Absent lower eyelashes
Synonym: Absent lower eyelashes; Agenesis of lower eyelashes; Aplasia of lower eyelashes; Atrichia of lower eyelashes; Failure of development of lower eyelashes
Definition: Lack of eyelashes on the lower lid.
Comments:
Reference: HP:0007646
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent inner eyelashes (HP:0007708) help
..expandAbsent upper eyelashes (HP:0040056) 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:0007646HP:0007646Absent lower eyelashes0SF3B4 CL E G H1026210771OMIM:154400Acrofacial dysostosis 1, Nager type49
HP:0007646HP:0007646Absent lower eyelashes0TWIST2 CL E G H11758120670OMIM:227260FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE; FFDD37


Genes (2) :SF3B4 TWIST2

Diseases (2) :OMIM:154400 OMIM:227260
 

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