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Osteosarcoma
1 OMIM reference -
1 associated gene
65 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary breast and ovarian cancer syndrome
Familial prostate cancer
Li-Fraumeni syndrome
Familial pancreatic carcinoma
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
B-cell chronic lymphocytic leukemia
Primary peritoneal carcinoma
Constitutional mismatch repair deficiency syndrome
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Adrenocortical carcinoma
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Nijmegen breakage syndrome-like disorder
Fanconi anemia
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia type 12
Ataxia-telangiectasia
Ataxia-telangiectasia variant
Combined cervical dystonia
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Mantle cell lymphoma
Seckel syndrome
Acute promyelocytic leukemia
Chuvash erythrocytosis
Von Hippel-Lindau disease
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Chronic mucocutaneous candidiasis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Spondylocarpotarsal synostosis
Susceptibility to viral and mycobacterial infections
Nijmegen breakage syndrome
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
COFS syndrome
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
Severe combined immunodeficiency due to DNA-PKcs deficiency
UV-sensitive syndrome
Synonym(s):
- Osteogenic sarcoma
Classification (Orphanet):
- Rare bone disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D012516
Gene symbol UniProt reference OMIM reference
CHEK2 O96017604373
No signs/symptoms info available.