Human Phenotype Ontology 
Grandparent Node:
Abnormal eye physiology (HP:0012373)help
Parent Node:
Ptosis (HP:0000508)help
..Starting node
Progressive ptosis (HP:0007838)help
Term ID: 7838
Name: Progressive ptosis
Synonym: Progressive drooping of upper eyelid
Definition: A progressive form of ptosis.
Reference: HP:0007838
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandBilateral ptosis (HP:0001488) help
..expandCongenital ptosis (HP:0007970) help
..expandHorner syndrome (HP:0002277) help
..expandUnilateral ptosis (HP:0007687) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0007838HP:0007838Progressive ptosis0PABPN1 CL E G H8106164300Oculopharyngeal muscular dystrophy164300C0270952OMIM1618565602279
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :PABPN1

Diseases (1) :164300

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.