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
Ulnar deviation of thumb
Symptom Information:
Symptom ID:
HPO:0006156
Synonyms:
Ulnar deviation of the 1st finger [HPO:0006156]
Quality:
Cross references:
Is a (Direct Parents):
HPO
Ulnar deviation of finger
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of the skeletal system(HPO:0000924)
Abnormality of skeletal morphology(HPO:0011842)
Abnormal appendicular skeleton morphology(HPO:0011844)
Abnormality of limb bone morphology(HPO:0002813)
Abnormality of the upper limb(HPO:0002817)
Abnormality of the hand(HPO:0001155)
Deviation of the hand or of fingers of the hand(HPO:0009484)
Ulnar deviation of the hand or of fingers of the hand(HPO:0001193)
Ulnar deviation of finger(HPO:0009465)
Ulnar deviation of thumb(HPO:0006156)
Deviation of finger(HPO:0004097)
Ulnar deviation of finger(HPO:0009465)
Ulnar deviation of thumb(HPO:0006156)
Abnormality of finger(HPO:0001167)
Deviation of finger(HPO:0004097)
Ulnar deviation of finger(HPO:0009465)
Ulnar deviation of thumb(HPO:0006156)
Abnormality of digit(HPO:0011297)
Abnormality of finger(HPO:0001167)
Deviation of finger(HPO:0004097)
Ulnar deviation of finger(HPO:0009465)
Ulnar deviation of thumb(HPO:0006156)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
WT limb-blood syndrome
(Orphanet:3466)