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Solitary fibrous tumor
1 OMIM reference -
2 associated genes
33 connected diseases
No signs/symptoms info
Disease Type of connection
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Herpetic encephalitis
Autosomal dominant hyper-IgE syndrome
Charcot-Marie-Tooth disease type 1C
Translocation renal cell carcinoma
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Familial pancreatic carcinoma
Familial partial lipodystrophy due to AKT2 mutations
Giant cell glioblastoma
Gliosarcoma
Hereditary combined deficiency of vitamin K-dependent clotting factors
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Li-Fraumeni syndrome
Papillary or follicular thyroid carcinoma
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Recurrent infection due to specific granule deficiency
Spondylometaphyseal dysplasia - cone-rod dystrophy
T-B+ severe combined immunodeficiency due to JAK3 deficiency
Charcot-Marie-Tooth disease type 1D
Charcot-Marie-Tooth disease type 4E
Dejerine-Sottas syndrome
Idiopathic aplastic anemia
Anaplastic ependymoma
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia
Phosphoserine aminotransferase deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D006393
Gene symbol UniProt reference OMIM reference
NAB2 Q15742602381
STAT6 P42226601512
No signs/symptoms info available.