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
Lipomas of the central neryous system
Symptom Information:
Symptom ID:
HPO:0100251
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO
Multiple lipomas
HPO
Benign neoplasm of the central nervous system
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Neoplasm(HPO:0002664)
Neoplasm by anatomical site(HPO:0011793)
Neoplasm of fatty tissue(HPO:0200013)
Lipomatous tumor(HPO:0012031)
Multiple lipomas(HPO:0001012)
Lipomas of the central neryous system(HPO:0100251)
Neoplasm of the nervous system(HPO:0004375)
Neoplasm of the central nervous system(HPO:0100006)
Benign neoplasm of the central nervous system(HPO:0100835)
Lipomas of the central neryous system(HPO:0100251)
Abnormality of the nervous system(HPO:0000707)
Abnormality of nervous system morphology(HPO:0012639)
Morphological abnormality of the central nervous system(HPO:0002011)
Neoplasm of the central nervous system(HPO:0100006)
Benign neoplasm of the central nervous system(HPO:0100835)
Lipomas of the central neryous system(HPO:0100251)
Neoplasm of the nervous system(HPO:0004375)
Neoplasm of the central nervous system(HPO:0100006)
Benign neoplasm of the central nervous system(HPO:0100835)
Lipomas of the central neryous system(HPO:0100251)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Encephalocraniocutaneous lipomatosis
(Orphanet:2396)