Human Phenotype Ontology 
Grandparent Node:
obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
Abnormal sclera morphology (HP:0000591)help
..Starting node
Pigmentation of the sclera (HP:0007832)help
Term ID: 7832
Name: Pigmentation of the sclera
Synonym: Pigmentation of the outer white part of the eyeball
Reference: HP:0007832
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
..expandScleral rupture (HP:0025513) 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:0007832HP:0007832Pigmentation of the sclera0HGD CL E G H30814892OMIM:203500Alkaptonuria.77
HP:0007832HP:0007832Pigmentation of the sclera0PRKAR1A CL E G H55739388OMIM:160980Carney complex, type 1134

Genes (2) :HGD PRKAR1A

Diseases (2) :OMIM:203500 OMIM:160980

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