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Myeloid neoplasm associated with PDGFRA rearrangement
1 associated gene
66 connected diseases
No signs/symptoms info
Disease Type of connection
Idiopathic hypereosinophilic syndrome
Gastrointestinal stromal tumor
Precursor B-cell acute lymphoblastic leukemia
Bilateral striopallidodentate calcinosis
Juvenile myelomonocytic leukemia
Chronic myelomonocytic leukemia
Dermatofibrosarcoma protuberans
Familial multiple meningioma
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRB rearrangement
Unclassified chronic myeloproliferative disease
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Distal 22q11.2 microdeletion syndrome
Autosomal agammaglobulinemia
Autosomal dominant limb-girdle muscular dystrophy type 1C
Rippling muscle disease
Romano-Ward syndrome
SHORT syndrome
Autosomal dominant macrothrombocytopenia
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
Acute myeloblastic leukemia with maturation
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Aleukemic mast cell leukemia
Bannayan-Riley-Ruvalcaba syndrome
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cowden syndrome
Cutaneous mastocytoma
Familial thoracic aortic aneurysm and aortic dissection
Hereditary breast and ovarian cancer syndrome
Hereditary nonpolyposis colon cancer
Isolated bone marrow mastocytosis
Juvenile polyposis of infancy
Lhermitte-Duclos disease
Loeys-Dietz syndrome type 1
Lymphoadenopathic mastocytosis with eosinophilia
Macrocephaly-autism syndrome
Marfan syndrome type 2
Nodular urticaria pigmentosa
Piebaldism
Plaque-form urticaria pigmentosa
Proteus syndrome
Proteus-like syndrome
Pseudoxanthomatous diffuse cutaneous mastocytosis
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Smouldering systemic mastocytosis
Squamous cell carcinoma of head and neck
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Acute promyelocytic leukemia
Autosomal dominant hyper-IgE syndrome
Chronic mucocutaneous candidiasis
Laron syndrome with immunodeficiency
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
PDGFRA P16234173490
No signs/symptoms info available.