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
Symmetric spinal nerve root neurofibromas
Symptom Information:
Symptom ID:
HPO:0006851
Synonyms:
Spinal nerve root neurofibromas, symmetric, multiple [HPO:0006851]
Spinal nerve root neurofibromas, symmetric, multiple [OMIM:Spinal nerve root neurofibromas, symmetric, multiple]
Quality:
Cross references:
OMIM: "Spinal nerve root neurofibromas, symmetric, multiple" [OMIM:Spinal nerve root neurofibromas, symmetric, multiple]
Is a (Direct Parents):
HPO
Spinal neurofibromas
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of the nervous system(HPO:0000707)
Neoplasm of the nervous system(HPO:0004375)
Neoplasm of the peripheral nervous system(HPO:0100007)
Neurofibromas(HPO:0001067)
Spinal neurofibromas(HPO:0009735)
Symmetric spinal nerve root neurofibromas(HPO:0006851)
Abnormality of nervous system morphology(HPO:0012639)
Abnormal peripheral nervous system morphology(HPO:0000759)
Neoplasm of the peripheral nervous system(HPO:0100007)
Neurofibromas(HPO:0001067)
Spinal neurofibromas(HPO:0009735)
Symmetric spinal nerve root neurofibromas(HPO:0006851)
Abnormality of the integument(HPO:0001574)
Abnormality of the skin(HPO:0000951)
Neoplasm of the skin(HPO:0008069)
Neurofibromas(HPO:0001067)
Spinal neurofibromas(HPO:0009735)
Symmetric spinal nerve root neurofibromas(HPO:0006851)
Neoplasm(HPO:0002664)
Neoplasm by anatomical site(HPO:0011793)
Neoplasm of the nervous system(HPO:0004375)
Neoplasm of the peripheral nervous system(HPO:0100007)
Neurofibromas(HPO:0001067)
Spinal neurofibromas(HPO:0009735)
Symmetric spinal nerve root neurofibromas(HPO:0006851)
Neoplasm of the skin(HPO:0008069)
Neurofibromas(HPO:0001067)
Spinal neurofibromas(HPO:0009735)
Symmetric spinal nerve root neurofibromas(HPO:0006851)
Neoplasm by histology(HPO:0011792)
Fibrous tissue neoplasm(HPO:0012316)
Fibroma(HPO:0010614)
Neurofibromas(HPO:0001067)
Spinal neurofibromas(HPO:0009735)
Symmetric spinal nerve root neurofibromas(HPO:0006851)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
NEUROFIBROMATOSIS, FAMILIAL SPINAL
(OMIM:162210)