Human Phenotype Ontology 
Grandparent Node:
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Abnormality of globe size (HP:0100887)help
Grandparent Node:
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Aplasia/Hypoplasia affecting the eye (HP:0008056)help
Parent Node:
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Microphthalmia (HP:0000568)help
..Starting node
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Unilateral microphthalmos (HP:0011480)help
Term ID: 11480
Name: Unilateral microphthalmos
Synonym: Abnormally small eyeball on one side; Unilateral nanophthalmos
Definition: A developmental anomaly characterized by abnormal smallness of one eye.
Comments:
Reference: HP:0011480
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilateral microphthalmos (HP:0007633) 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:0011480HP:0011480Unilateral microphthalmos0CAPN15 CL E G H665011182OMIM:619318OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME; OGIN
HP:0011480HP:0011480Unilateral microphthalmos0CHD7 CL E G H5563620626OMIM:214800Charge syndrome515
HP:0011480HP:0011480Unilateral microphthalmos0PAX6 CL E G H50808620ORPHA:137902Isolated optic nerve hypoplasia/aplasiaHP:0040283 - Occasional194


Genes (3) :CAPN15 CHD7 PAX6

Diseases (3) :OMIM:619318 OMIM:214800 ORPHA:137902
 

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