Human Phenotype Ontology 
Grandparent Node:
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Abnormality iris morphology (HP:0000525)help
Parent Node:
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Abnormal pupil morphology (HP:0000615)help
..Starting node
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Microcoria (HP:0025492)help
Term ID: 25492
Name: Microcoria
Synonym:
Definition: A small pupil (typically diameter less than 2 mm) that dilates poorly or not at all in response to topically administered mydriatic drugs.
Comments:
Reference: HP:0025492
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal pupil shape (HP:0025309) help
..expandAnisocoria (HP:0009916) help
..expandEctopia pupillae (HP:0009918) help
..expandLeukocoria (HP:0000555) help
..expandPersistent pupillary membrane (HP:0009917) help
..expandPolycoria (HP:0011500) 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:0025492HP:0025492Microcoria0GFAP CL E G H26704235OMIM:203450Alexander disease188
HP:0025492HP:0025492Microcoria0LAMB2 CL E G H39136487OMIM:609049Pierson syndrome.92
HP:0025492HP:0025492Microcoria0RBP4 CL E G H59509922OMIM:616428Microphthalmia, isolated, with coloboma 10HP:0040283 - Occasional8
HP:0025492HP:0025492Microcoria0TONSL CL E G H47967801ORPHA:93357SPONASTRIME dysplasiaHP:0040283 - Occasional


Genes (4) :GFAP LAMB2 RBP4 TONSL

Diseases (4) :OMIM:203450 OMIM:609049 OMIM:616428 ORPHA:93357
 

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