Human Phenotype Ontology 
Grandparent Node:
obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
Abnormal sclera morphology (HP:0000591)help
..Starting node
Scleral rupture (HP:0025513)help
Term ID: 25513
Name: Scleral rupture
Definition: Breakage of the sclera.
Reference: HP:0025513
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandBlue sclerae (HP:0000592) help
..expandDeep episcleral hyperemia (HP:0025340) help
..expandEpiscleritis (HP:0100534) help
..expandLimbal dermoid (HP:0001140) help
..expandOcular melanocytosis (HP:0025534) help
..expandPigmentation of the sclera (HP:0007832) help
..expandScleral schwannoma (HP:0100011) help
..expandScleral staphyloma (HP:0030854) help
..expandScleral thickening (HP:0030823) help
..expandScleritis (HP:0100532) help
..expandSuperficial episcleral hyperemia (HP:0025339) 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:0025513HP:0025513Scleral rupture0PLOD1 CL E G H53519081ORPHA:1900Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiencyHP:0040283 - Occasional105

Genes (1) :PLOD1

Diseases (1) :ORPHA:1900

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