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Acute myeloblastic leukemia with maturation
3 associated genes
224 connected diseases
No signs/symptoms info
Disease Type of connection
Acute myeloblastic leukemia without 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
Acute myelomonocytic leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Acute promyelocytic leukemia
Gastrointestinal stromal tumor
Acute biphenotypic leukemia
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cutaneous mastocytoma
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Minimally differentiated acute myeloblastic leukemia
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
Juvenile myelomonocytic leukemia
Autosomal agammaglobulinemia
Familial pancreatic carcinoma
SHORT syndrome
Inflammatory myofibroblastic tumor
Amyotrophic lateral sclerosis
Young adult-onset Parkinsonism
Essential thrombocythemia
LEOPARD syndrome
Noonan syndrome
Dedifferentiated liposarcoma
Distal 22q11.2 microdeletion syndrome
Well-differentiated liposarcoma
Hereditary breast and ovarian cancer syndrome
Chronic myeloid leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Chronic mucocutaneous candidiasis
Common variable immunodeficiency
Translocation renal cell carcinoma
Behavioral variant of frontotemporal dementia
Fanconi anemia
Progressive non-fluent aphasia
Semantic dementia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
PLCG2-associated antibody deficiency and immune dysregulation
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Retinitis pigmentosa
Congenital pulmonary alveolar proteinosis
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Familial progressive hyper- and hypopigmentation
Familial progressive hyperpigmentation
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Testicular non seminomatous germ cell tumor
Testicular seminomatous germ cell tumor
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Severe combined immunodeficiency due to LCK deficiency
Anaplastic ependymoma
Budd-Chiari syndrome
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Estrogen resistance syndrome
Branchio-oculo-facial syndrome
Familial melanoma
Familial prostate cancer
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Primary peritoneal carcinoma
Susceptibility to viral and mycobacterial infections
Congenital communicating hydrocephalus
Cowden syndrome
Ear-patella-short stature syndrome
Proteus syndrome
12q14 microdeletion syndrome
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Miller-Dieker syndrome
46,XY complete gonadal dysgenesis
Combined immunodeficiency due to ZAP70 deficiency
Fibronectin glomerulopathy
MODY syndrome
X-linked lymphoproliferative disease
Multiple endocrine neoplasia type 1
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Ewing sarcoma
Extraskeletal Ewing sarcoma
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Peripheral primitive neuroectodermal tumor
Primary familial polycythemia
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Cone rod dystrophy
Laron syndrome with immunodeficiency
Omenn syndrome
Primary ciliary dyskinesia
Primary ciliary dyskinesia - retinitis pigmentosa
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
Acrodysostosis with multiple hormone resistance
Adult-onset distal myopathy due to VCP mutation
Adult-onset foveomacular vitelliform dystrophy
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Autosomal dominant Larsen syndrome
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal dominant secondary polycythemia
Autosomal recessive nonsyndromic intellectual deficit
Autosomal recessive primary microcephaly
Blackfan-Diamond anemia
Boomerang dysplasia
CLN11 disease
Cardiomyopathy - hypotonia - lactic acidosis
Carney complex
Chronic intestinal pseudoobstruction
Coffin-Siris syndrome
Combined oxidative phosphorylation defect type 4
Congenital fibrosis of extraocular muscles
Congenital short bowel syndrome
Congenital valvular dysplasia
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Distal hereditary motor neuropathy type 2
Distal myopathy with posterior leg and anterior hand involvement
Dubowitz syndrome
Ehlers-Danlos syndrome with periventricular heterotopia
Erythrocyte galactose epimerase deficiency
Familial atrial myxoma
Familial capillary hemangioma
Familial infantile bilateral striatal necrosis
Familial multinodular goiter
Familial retinoblastoma
Familial rhabdoid tumor
Frontometaphyseal dysplasia
Frontotemporal dementia with motor neuron disease
Generalized congenital lipodystrophy with myopathy
Generalized galactose epimerase deficiency
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hereditary thrombophilia due to congenital protein S deficiency
Idiopathic hypereosinophilic syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
Isolated ATP synthase deficiency
Isolated growth hormone deficiency type IA
Isolated growth hormone deficiency type IB
Isolated growth hormone deficiency type II
LAMB-2-related infantile-onset nephrotic syndrome
Microcephaly - lymphedema - chorioretinopathy
Monosomy 13q14
Multiple paragangliomas associated with polycythemia
Muscle filaminopathy
Myeloid neoplasm associated with PDGFRA rearrangement
Neurological conditions associated with aminoacylase 1 deficiency
Obesity due to melanocortin 4 receptor deficiency
Oculopharyngeal muscular dystrophy
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Ovarian malignant Sertoli-Leydig cell tumor
Papillary or follicular thyroid carcinoma
Periventricular nodular heterotopia
Pierson syndrome
Pleuropulmonary blastoma family tumor susceptibility syndrome
Primary pigmented nodular adrenocortical disease
Proximal myotonic myopathy
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Pseudohypoaldosteronism type 2E
Pyruvate carboxylase deficiency, benign type
Pyruvate carboxylase deficiency, infantile type
Pyruvate carboxylase deficiency, severe neonatal type
Seckel syndrome
Short stature due to growth hormone qualitative anomaly
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia type 26
Spinocerebellar ataxia type 36
Spondylocarpotarsal synostosis
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Synaptic congenital myasthenic syndromes
Terminal osseous dysplasia - pigmentary defects
Unilateral retinoblastoma
X-linked Opitz G / BBB syndrome
Legius 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
ALK-positive anaplastic large cell lymphoma
ALK-positive large B-cell lymphoma
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
T-B+ severe combined immunodeficiency due to JAK3 deficiency
X-linked agammaglobulinemia
Glycogen storage disease due to LAMP-2 deficiency
- Acute myeloblastic leukemia type 2

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

Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
FLT3 P36888136351
KIT P10721164920
NPM1 P06748164040
No signs/symptoms info available.