Human Phenotype Ontology 
Grandparent Node:
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Opacification of the corneal stroma (HP:0007759)help
Parent Node:
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Punctate opacification of the cornea (HP:0007856)help
..Starting node
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Crystalline corneal dystrophy (HP:0007760)help
Term ID: 7760
Name: Crystalline corneal dystrophy
Synonym:
Definition:
Comments:
Reference: HP:0007760
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007760HP:0007760Crystalline corneal dystrophy0UBIAD1 CL E G H29914121800Schnyder crystalline corneal dystrophy121800C0271287OMIM13014430791611632
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :UBIAD1

Diseases (1) :121800
 

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