Human Phenotype Ontology 
Grandparent Node:
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obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
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Abnormal uvea morphology (HP:0000553)help
..Starting node
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Abnormal ciliary body morphology (HP:0012776)help
Term ID: 12776
Name: Abnormal ciliary body morphology
Synonym: Abnormality of the ciliary body
Definition: A structural anomaly of the ciliary body.
Comments:
Reference: HP:0012776
Genes and Diseases:
 
       Child Nodes:
........expandHypoplasia of the ciliary body (HP:0007774) help
........expandCiliary body melanoma (HP:0012055) help

 Sister Nodes: 
..expandAbnormal choroid morphology (HP:0000610) help
..expandAbnormality iris morphology (HP:0000525) help
..expandAplasia/Hypoplasia affecting the uvea (HP:0008055) 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:0012776HP:0012776Abnormal ciliary body morphology0 CL E G H
HP:0012776HP:0012776Abnormal ciliary body morphology1 CL E G H


Genes (6) :BAP1 CYSLTR2 GNA11 GNAQ LAMB2 SF3B1

Diseases (2) :39044 609049
 

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