Human Phenotype Ontology 
Grandparent Node:
obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
Abnormal sclera morphology (HP:0000591)help
..Starting node
Scleral thickening (HP:0030823)help
Term ID: 30823
Name: Scleral thickening
Synonym: Thick sclera
Definition: Increased dimension of the sclera in the anterior-posterior axis.
Reference: HP:0030823
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 rupture (HP:0025513) help
..expandScleral schwannoma (HP:0100011) help
..expandScleral staphyloma (HP:0030854) 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:0030823HP:0030823Scleral thickening0IDS CL E G H34235389ORPHA:217093Mucopolysaccharidosis type 2, attenuated formHP:0040283 - Occasional86
HP:0030823HP:0030823Scleral thickening0IDS CL E G H34235389ORPHA:217085Mucopolysaccharidosis type 2, severe formHP:0040283 - Occasional86
HP:0030823HP:0030823Scleral thickening0MFRP CL E G H8355218121OMIM:611040Microphthalmia, isolated 5.26
HP:0030823HP:0030823Scleral thickening0PRSS56 CL E G H64696039433OMIM:613517Microphthalmia, isolated 6.11

Genes (3) :IDS MFRP PRSS56

Diseases (4) :ORPHA:217093 ORPHA:217085 OMIM:611040 OMIM:613517

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