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PedAM

Pediatric Disease Annotations & Medicines



   chondromyxoid fibroma
  

Disease ID 1679
Disease chondromyxoid fibroma
Definition
An uncommon benign cartilaginous neoplasm arising from the bone. It is characterized by the presence of spindle-shaped or stellate chondrocytes, a lobulated growth pattern, myxoid stroma formation, and sometimes multinucleated giant cells. It has been associated with chromosomal rearrangement of 6q13 and 6q25 bands. The most common clinical symptom is mild, localized pain.
Synonym
chondromyxoid fibroma (morphologic abnormality)
cmf - chondromyxoid fibroma
fibroma, chondromyxoid
Orphanet
UMLS
C0221290
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:2)
C0017525  |  giant cell tumor  |  1
C1334699  |  mesenchymal tumor  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
GRM1  |  2911  |  ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus
Symbol | Locus(Total Locus:1)
GRM1  |  6q24.3
Disease ID 1679
Disease chondromyxoid fibroma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:4)
HP:0012063  |  Aneurysmal bone cyst  |  2
HP:0012062  |  Bone cysts  |  2
HP:0011847  |  Giant cell tumor of bone  |  1
HP:0002664  |  Neoplasia  |  1
Disease ID 1679
Disease chondromyxoid fibroma
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)