Human Phenotype Ontology 
Grandparent Node:
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Abnormal cornea morphology (HP:0000481)help
Parent Node:
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Corneal dystrophy (HP:0001131)help
..Starting node
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Granular corneal dystrophy (HP:0007802)help
Term ID: 7802
Name: Granular corneal dystrophy
Synonym:
Definition: The presence of central, fine, whitish granular lesions in the stroma of the cornea. This type of corneal dystrophy is usually asymptomatic and begins in childhood and shows a slow progression. Later in the course, the corneal epithelium and Bowman's layer may be affected. Histologically, the cornea shows a uniform deposition of hyaline material.
Comments:
Reference: HP:0007802
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBand-shaped corneal dystrophy (HP:0007709) help
..expandCongenital corneal dystrophy (HP:0008005) help
..expandLattice corneal dystrophy (HP:0001149) help
..expandMarginal corneal dystrophy (HP:0007880) help
..expandMosaic corneal dystrophy (HP:0007836) help
..expandPunctate corneal dystrophy (HP:0007809) help
..expandSpeckled corneal dystrophy (HP:0007962) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007802HP:0007802Granular corneal dystrophy0TGFBI CL E G H7045121900Groenouw corneal dystrophy type I121900C1641846OMIM17011911771601692
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :TGFBI

Diseases (1) :121900
 

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