Human Phenotype Ontology 
Grandparent Node:
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Abnormal eye physiology (HP:0012373)help
Parent Node:
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Ptosis (HP:0000508)help
..Starting node
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Progressive ptosis (HP:0007838)help
Term ID: 7838
Name: Progressive ptosis
Synonym: Progressive drooping of upper eyelid
Definition: A progressive form of ptosis.
Comments:
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 dystrophy164300C0270952OMIM123518565602279
 
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 June 2019 release.