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Chronic myelomonocytic leukemia
2 associated genes
100 connected diseases
No signs/symptoms info
Disease Type of connection
Idiopathic hypereosinophilic syndrome
Precursor B-cell acute lymphoblastic leukemia
Bilateral striopallidodentate calcinosis
Congenital mesoblastic nephroma
Fibrosarcoma
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRB rearrangement
Unclassified chronic myeloproliferative disease
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
LEOPARD syndrome
Noonan syndrome
Juvenile myelomonocytic leukemia
Cowden syndrome
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
Distal 22q11.2 microdeletion syndrome
Metachondromatosis
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Autosomal agammaglobulinemia
Gastrointestinal stromal tumor
Myeloid neoplasm associated with PDGFRA rearrangement
SHORT syndrome
Capillary malformation - arteriovenous malformation
Dermatofibrosarcoma protuberans
Familial multiple meningioma
Parkes Weber syndrome
Pilocytic astrocytoma
Bannayan-Riley-Ruvalcaba syndrome
Hereditary breast and ovarian cancer syndrome
Juvenile polyposis of infancy
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Proteus syndrome
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Squamous cell carcinoma of head and neck
Giant cell glioblastoma
Gliosarcoma
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Ewing sarcoma
Extraskeletal Ewing sarcoma
Heritable pulmonary arterial hypertension
Isolated delta-storage pool disease
Limited cutaneous systemic sclerosis
Paris-Trousseau thrombocytopenia
Peripheral primitive neuroectodermal tumor
Peters anomaly
Autosomal dominant limb-girdle muscular dystrophy type 1C
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Rippling muscle disease
Romano-Ward syndrome
Autosomal dominant macrothrombocytopenia
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Giant cell arteritis
Granulomatosis with polyangiitis
Pediatric systemic lupus erythematosus
T-B+ severe combined immunodeficiency due to CD45 deficiency
Chronic mucocutaneous candidiasis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Anophthalmia / microphthalmia - esophageal atresia
Burkitt lymphoma
Colobomatous microphthalmia
Distal myopathy with posterior leg and anterior hand involvement
Herpetic encephalitis
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Isolated anophthalmia - microphthalmia
Muscle filaminopathy
Precursor T-cell acute lymphoblastic leukemia
Septo-optic dysplasia
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Autosomal dominant nonsyndromic intellectual deficit
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Acute promyelocytic leukemia
Autosomal dominant hyper-IgE syndrome
CLOVE syndrome
Hemimegalencephaly
Hereditary nonpolyposis colon cancer
Laron syndrome with immunodeficiency
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D015477
Gene symbol UniProt reference OMIM reference
ETV6 P41212600618
PDGFRB P09619173410
No signs/symptoms info available.