chondromyxoid fibroma |
Disease ID | 1679 |
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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) |
Curated Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | (Waiting for update.) |
Locus | Symbol | Locus(Total Locus:1) GRM1 | 6q24.3 |
Disease ID | 1679 |
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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 |
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Disease | chondromyxoid fibroma |
Manually Symptom | (Waiting for update.) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Chemical(Total Drugs:0) | |
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(Waiting for update.) |
FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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(Waiting for update.) |