Human Phenotype Ontology 
Grandparent Node:
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Abnormal uvea morphology (HP:0000553)help
Grandparent Node:
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Aplasia/Hypoplasia affecting the eye (HP:0008056)help
Parent Node:
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Abnormal ciliary body morphology (HP:0012776)help
Parent Node:
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Aplasia/Hypoplasia affecting the uvea (HP:0008055)help
..Starting node
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Hypoplasia of the ciliary body (HP:0007774)help
Term ID: 7774
Name: Hypoplasia of the ciliary body
Synonym:
Definition: Underdevelopment of the ciliary body.
Comments:
Reference: HP:0007774
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia of the iris (HP:0008053) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007774HP:0007774Hypoplasia of the ciliary body0LAMB2 CL E G H3913609049Pierson syndrome609049C1836876OMIM11273686487150325
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :LAMB2

Diseases (1) :609049
 

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