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
Vitamin E deficiency
Symptom Information:
Symptom ID:
HPO:0100513
Synonyms:
Vitamin E deficiency (disorder) [Orphanet:49840]
Vitamin E Deficiency [Orphanet:49840]
Vitamin E deficiency [Orphanet:49840]
Vitamin E deficiency [MedDRA:10047631]
Tocopherol deficiency [MedDRA:10047631]
Quality:
Cross references:
Orphanet:49840 "Vitamin E deficiency" [Orphanet:49840]
UMLS:C0042875 "Vitamin E Deficiency" [Orphanet:49840]
Is a (Direct Parents):
MedDRA
Fat soluble vitamin deficiencies and disorders
Orphanet
Abnormality of vitamin metabolism
HPO
Abnormality of vitamin E metabolism
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of metabolism/homeostasis(HPO:0001939)
Abnormality of vitamin metabolism(HPO:0100508)
Abnormality of vitamin E metabolism(HPO:0100514)
Vitamin E deficiency(HPO:0100513)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
Vitamin related disorders(MedDRA:10047635)
Fat soluble vitamin deficiencies and disorders(MedDRA:10016250)
Vitamin E deficiency(HPO:0100513)
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Ataxia with vitamin E deficiency
(Orphanet:96)