Human Phenotype Ontology 
Grandparent Node:
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Opacification of the corneal stroma (HP:0007759)help
Parent Node:
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Generalized opacification of the cornea (HP:0011494)help
..Starting node
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Nodular corneal dystrophy (HP:0007827)help
Term ID: 7827
Name: Nodular corneal dystrophy
Synonym:
Definition:
Comments:
Reference: HP:0007827
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007827HP:0007827Nodular 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.