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
Adductor longus contractures
Symptom Information:
Symptom ID:
HPO:0006366
Synonyms:
Adductor longus contractures [OMIM:Adductor longus contractures]
Quality:
Cross references:
OMIM: "Adductor longus contractures" [OMIM:Adductor longus contractures]
Is a (Direct Parents):
HPO
Contractures of the joints of the lower limbs
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 joint morphology(HPO:0001367)
Abnormality of joint mobility(HPO:0011729)
Flexion contracture(HPO:0001371)
Limb joint contracture(HPO:0003121)
Contractures of the joints of the lower limbs(HPO:0005750)
Adductor longus contractures(HPO:0006366)
Abnormality of connective tissue(HPO:0003549)
Flexion contracture(HPO:0001371)
Limb joint contracture(HPO:0003121)
Contractures of the joints of the lower limbs(HPO:0005750)
Adductor longus contractures(HPO:0006366)
Abnormality of the musculature(HPO:0003011)
Abnormality of muscle morphology(HPO:0011805)
Flexion contracture(HPO:0001371)
Limb joint contracture(HPO:0003121)
Contractures of the joints of the lower limbs(HPO:0005750)
Adductor longus contractures(HPO:0006366)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Behr syndrome
(Orphanet:1239)