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Juvenile myelomonocytic leukemia
1 OMIM reference -
5 associated genes
304 connected diseases
No signs/symptoms info
Disease Type of connection
Noonan syndrome
LEOPARD syndrome
Pilocytic astrocytoma
Hereditary nonpolyposis colon cancer
Costello syndrome
Linear nevus sebaceus syndrome
Familial pancreatic carcinoma
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
17q11 microdeletion syndrome
17q11.2 microduplication syndrome
Autoimmune lymphoproliferative syndrome
Cardiofaciocutaneous syndrome
Large congenital melanocytic nevus
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion
Watson syndrome
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Distal 22q11.2 microdeletion syndrome
Idiopathic hypereosinophilic syndrome
Hepatocellular carcinoma, childhood-onset
Gastrointestinal stromal tumor
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
Cowden syndrome
Autosomal dominant nonsyndromic intellectual deficit
Familial medullary thyroid carcinoma
Papillary or follicular thyroid carcinoma
Epidermolytic palmoplantar keratoderma
Pachyonychia congenita
Autosomal agammaglobulinemia
Infantile myofibromatosis
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
CLOVE syndrome
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Chronic myeloid leukemia
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Hereditary spherocytosis
Acute promyelocytic leukemia
Giant cell glioblastoma
Familial papillary renal cell carcinoma
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Myeloid neoplasm associated with PDGFRB rearrangement
SHORT syndrome
Unclassified chronic myeloproliferative disease
Noonan syndrome-like disorder with loose anagen hair
Growth delay due to insulin-like growth factor I resistance
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cutaneous mastocytoma
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Nodular urticaria pigmentosa
Plaque-form urticaria pigmentosa
Pseudoxanthomatous diffuse cutaneous mastocytosis
Smouldering systemic mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Severe combined immunodeficiency due to LCK deficiency
Posterior polar cataract
Total congenital cataract
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Limited cutaneous systemic sclerosis
Rabson-Mendenhall syndrome
Catecholaminergic polymorphic ventricular tachycardia
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Primary familial polycythemia
Hereditary gingival fibromatosis
Myeloid neoplasm associated with PDGFRA rearrangement
Amyotrophic lateral sclerosis
Acute biphenotypic leukemia
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Familial capillary hemangioma
Minimally differentiated acute myeloblastic leukemia
Bilateral renal agenesis
Bilateral renal dysplasia
Haddad syndrome
Hirschsprung disease
Multiple endocrine neoplasia type 2A
Multiple endocrine neoplasia type 2B
Unilateral renal dysplasia
Desmoid tumor
Phakomatosis pigmentokeratotica
Intermittent hydrarthrosis
TRAPS syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Laron syndrome with immunodeficiency
Mucocutaneous venous malformations
Early-onset autosomal dominant Alzheimer disease
Granulomatosis with polyangiitis
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
Follicular lymphoma
Intravascular large B-cell lymphoma
Annular epidermolytic ichthyosis
Autosomal dominant macrothrombocytopenia
Childhood-onset nemaline myopathy
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Epidermolytic ichthyosis
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Intermediate nemaline myopathy
Localized epidermolysis bullosa simplex
Severe congenital nemaline myopathy
Squamous cell carcinoma of head and neck
Typical nemaline myopathy
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Autosomal dominant hypohidrotic ectodermal dysplasia
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
Budd-Chiari syndrome
Combined immunodeficiency due to ZAP70 deficiency
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Congenital pulmonary alveolar proteinosis
Obesity due to leptin receptor gene deficiency
Laron syndrome
Short stature due to partial GHR deficiency
MODY syndrome
Autosomal dominant hyper-IgE syndrome
Syndromic multisystem autoimmune disease due to Itch deficiency
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Kallmann syndrome
Normosmic congenital hypogonadotropic hypogonadism
Testicular non seminomatous germ cell tumor
Testicular seminomatous germ cell tumor
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive lymphoproliferative disease
X-linked distal arthrogryposis multiplex congenita
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Giant cell arteritis
Pediatric systemic lupus erythematosus
Baraitser-Winter syndrome
Congenital bilateral absence of vas deferens
Cystic fibrosis
Developmental malformations - deafness - dystonia
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Leber congenital amaurosis
PLCG2-associated antibody deficiency and immune dysregulation
Partial androgen insensitivity syndrome
Senior-Loken syndrome
Lethal congenital contracture syndrome type 2
Adult-onset distal myopathy due to VCP mutation
Behavioral variant of frontotemporal dementia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
T-B+ severe combined immunodeficiency due to CD45 deficiency
Atypical chronic myeloid leukemia
Chronic neutrophilic leukemia
Hereditary neutrophilia
Hyper-IgM syndrome type 3
WHIM syndrome
Anauxetic dysplasia
Antley-Bixler syndrome
Apert syndrome
Autosomal dominant distal renal tubular acidosis
Autosomal dominant secondary polycythemia
Autosomal recessive epidermolysis bullosa simplex
Bannayan-Riley-Ruvalcaba syndrome
Blackfan-Diamond anemia
Burkitt lymphoma
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
Coffin-Siris syndrome
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Congenital reticular ichthyosiform erythroderma
Crouzon disease
Cutis gyrata - acanthosis nigricans - craniosynostosis
Dedifferentiated liposarcoma
Dermatopathia pigmentosa reticularis
Distal renal tubular acidosis with anemia
Dowling-Degos disease
Early infantile epileptic encephalopathy
Epidermolysis bullosa simplex with circinate migratory erythema
FGFR2-related bent bone dysplasia
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Familial rhabdoid tumor
Familial scaphocephaly syndrome, McGillivray type
Familial visceral myopathy
Fetal Gaucher disease
Fetal and neonatal alloimmune thrombocytopenia
Gaucher disease - ophthalmoplegia - cardiovascular calcification
Gaucher disease type 1
Gaucher disease type 2
Gaucher disease type 3
Glanzmann thrombasthenia
Hereditary breast and ovarian cancer syndrome
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
Hyperparathyroidism - jaw tumor syndrome
Ichthyosis hystrix of Curth-Macklin
Jackson-Weiss syndrome
Juvenile polyposis of infancy
Keratosis palmoplantaris striata
Lacrimo-auriculo-dento-digital syndrome
Lhermitte-Duclos disease
Lissencephaly due to TUBA1A mutation
Macrocephaly-autism syndrome
Meesmann corneal dystrophy
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
Naegeli-Franceschetti-Jadassohn syndrome
Omenn syndrome
Parathyroid carcinoma
Pfeiffer syndrome type 1
Pfeiffer syndrome type 2
Pfeiffer syndrome type 3
Proteus syndrome
Proteus-like syndrome
Pulverulent cataract
Recessive X-linked ichthyosis
Saethre-Chotzen syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Southeast Asian ovalocytosis
Split hand-split foot malformation
Succinyl-CoA:3-ketoacid CoA transferase deficiency
Superficial epidermolytic ichthyosis
Syndromic X-linked ichthyosis
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
Well-differentiated liposarcoma
Wiskott-Aldrich syndrome
X-linked severe congenital neutropenia
X-linked thrombocytopenia with normal platelets
Young adult-onset Parkinsonism
West syndrome
Congenital intrinsic factor deficiency
Transcobalamin deficiency
Chronic mucocutaneous candidiasis
Familial expansile osteolysis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Osteopetrosis - hypogammaglobulinemia
Stüve-Wiedemann syndrome
Susceptibility to viral and mycobacterial infections
Williams syndrome
Atrial stand still
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Brugada syndrome
Common variable immunodeficiency
Congenital amegakaryocytic thrombocytopenia
Familial atrial fibrillation
Familial isolated dilated cardiomyopathy
Familial progressive cardiac conduction defect
Familial sick sinus syndrome
Fibrodysplasia ossificans progressiva
Idiopathic ventricular fibrillation, not Brugada type
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
Milroy disease
Romano-Ward syndrome
Aicardi-Goutières syndrome
Autosomal dominant spastic paraplegia type 13
Autosomal recessive limb-girdle muscular dystrophy type 2C
Gräsbeck-Imerslund disease
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
- Juvenile chronic myelomonocytic leukemia

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D054429

No signs/symptoms info available.