Human Phenotype Ontology 
Grandparent Node:
Abnormal eye physiology (HP:0012373)help
Grandparent Node:
Increased inflammatory response (HP:0012649)help
Parent Node:
Abnormal sclera morphology (HP:0000591)help
Parent Node:
Inflammatory abnormality of the eye (HP:0100533)help
..Starting node
Scleritis (HP:0100532)help
Term ID: 100532
Name: Scleritis
Synonym: Inflammation of the outer white part of the eye
Definition: Inflammation of the sclera.
Reference: HP:0100532
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandBlepharitis (HP:0000498) help
..expandConjunctivitis (HP:0000509) help
..expandEpiscleritis (HP:0100534) help
..expandKeratitis (HP:0000491) help
..expandUveitis (HP:0000554) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100532HP:0100532Scleritis0MBTPS2 CL E G H513602273Fara Chlupackova syndromeORPHA02615455300294

Genes (1) :MBTPS2

Diseases (1) :2273

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.