Home
Download
Help
Login
Standard Search
Auto Completion Symptom Search
Advanced Search
Field
Query
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Symptoms & Signs
Field
Query
Disease
Symptom
Kayser-Fleischer ring
Symptom Information:
Symptom ID:
HPO:0200032
Synonyms:
Fleischer's ring [HPO:0200032]
Fleischer-Kayser ring [HPO:0200032]
Fleischer-Struempell ring [HPO:0200032]
Kayser-Fleischer ring [OMIM:Kayser-Fleischer ring]
Fleischer ring [OMIM:Fleischer ring]
Kayser-Fleischer ring [MedDRA:10023321]
Quality:
Cross references:
OMIM: "Kayser-Fleischer ring" [OMIM:Kayser-Fleischer ring]
OMIM: "Fleischer ring" [OMIM:Fleischer ring]
Is a (Direct Parents):
MedDRA
Hepatobiliary signs and symptoms
HPO
Corneal opacity
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of the eye(HPO:0000478)
Abnormal eye morphology(HPO:0012372)
Abnormality of the globe(HPO:0012374)
Abnormality of the anterior segment of the globe(HPO:0004328)
Abnormality of the cornea(HPO:0000481)
Corneal opacity(HPO:0007957)
Kayser-Fleischer ring(HPO:0200032)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
Hepatic and hepatobiliary disorders(MedDRA:10019654)
Hepatobiliary signs and symptoms(MedDRA:10019709)
Kayser-Fleischer ring(HPO:0200032)
Database Frequency:
2 / 7739
Resource:
All diseases associated with this symptom:
KERATOCONUS 5
(OMIM:614622)
Wilson disease
(Orphanet:905)