Human Phenotype Ontology 
Grandparent Node:
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Corneal dystrophy (HP:0001131)help
Parent Node:
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Central corneal dystrophy (HP:0007881)help
Parent Node:
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Mosaic corneal dystrophy (HP:0007836)help
..Starting node
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Mosaic central corneal dystrophy (HP:0100690)help
Term ID: 100690
Name: Mosaic central corneal dystrophy
Synonym:
Definition:
Comments:
Reference: HP:0100690
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100690HP:0100690Mosaic central corneal dystrophy0 CL E G H


Genes (0) :

Diseases (0) :
 

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