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
Aplasia/Hypoplasia of the 3rd toe
Symptom Information:
Symptom ID:
HPO:0010331
Synonyms:
Absent/hypoplastic third toe [HPO:0010331]
Absent/hypoplastic third toe [OMIM:Absent/hypoplastic third toe]
Quality:
Cross references:
OMIM: "Absent/hypoplastic third toe" [OMIM:Absent/hypoplastic third toe]
Is a (Direct Parents):
HPO
Absent toe
HPO
Abnormality of the 3rd toe
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)
Aplasia/hypoplasia involving the skeleton(HPO:0009115)
Aplasia/hypoplasia of the extremities(HPO:0009815)
Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
Aplasia/Hypoplasia of toe(HPO:0001991)
Absent toe(HPO:0010760)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormal appendicular skeleton morphology(HPO:0011844)
Abnormality of limb bone morphology(HPO:0002813)
Aplasia/hypoplasia of the extremities(HPO:0009815)
Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
Aplasia/Hypoplasia of toe(HPO:0001991)
Absent toe(HPO:0010760)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormality of digit(HPO:0011297)
Abnormality of toe(HPO:0001780)
Aplasia/Hypoplasia of toe(HPO:0001991)
Absent toe(HPO:0010760)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormality of the 3rd toe(HPO:0010320)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormality of the lower limb(HPO:0002814)
Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
Aplasia/Hypoplasia of toe(HPO:0001991)
Absent toe(HPO:0010760)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormality of the foot(HPO:0001760)
Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
Aplasia/Hypoplasia of toe(HPO:0001991)
Absent toe(HPO:0010760)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormality of toe(HPO:0001780)
Aplasia/Hypoplasia of toe(HPO:0001991)
Absent toe(HPO:0010760)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
Abnormality of the 3rd toe(HPO:0010320)
Aplasia/Hypoplasia of the 3rd toe(HPO:0010331)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Townes-Brocks syndrome
(Orphanet:857)