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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Marginal corneal dystrophy (HP:0007880)help
Term ID: 7880
Name: Marginal corneal dystrophy
Synonym:
Definition:
Comments:
Reference: HP:0007880
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBand-shaped corneal dystrophy (HP:0007709) help
..expandCongenital corneal dystrophy (HP:0008005) help
..expandGranular corneal dystrophy (HP:0007802) help
..expandLattice corneal dystrophy (HP:0001149) 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:0007880HP:0007880Marginal corneal dystrophy0CYP4V2 CL E G H285440210370Bietti crystalline corneoretinal dystrophy210370C1859486OMIM110535823198608614
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :CYP4V2

Diseases (1) :210370
 

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