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
Metopic suture patent to nasal root
Symptom Information:
Symptom ID:
HPO:0005495
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO
Abnormality of the metopic suture
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of head or neck(HPO:0000152)
Abnormality of the head(HPO:0000234)
Abnormality of the skull(HPO:0000929)
Abnormality of the calvaria(HPO:0002683)
Abnormality of the fontanelles or cranial sutures(HPO:0000235)
Abnormality of cranial sutures(HPO:0011329)
Abnormality of the metopic suture(HPO:0005556)
Metopic suture patent to nasal root(HPO:0005495)
Abnormality of the face(HPO:0000271)
Abnormality of the forehead(HPO:0000290)
Abnormality of the metopic suture(HPO:0005556)
Metopic suture patent to nasal root(HPO:0005495)
Abnormality of the skeletal system(HPO:0000924)
Abnormality of skeletal morphology(HPO:0011842)
Abnormal axial skeleton morphology(HPO:0009121)
Abnormality of the skull(HPO:0000929)
Abnormality of the calvaria(HPO:0002683)
Abnormality of the fontanelles or cranial sutures(HPO:0000235)
Abnormality of cranial sutures(HPO:0011329)
Abnormality of the metopic suture(HPO:0005556)
Metopic suture patent to nasal root(HPO:0005495)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Schinzel-Giedion syndrome
(Orphanet:798)