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Acute myelomonocytic leukemia
2 associated genes
174 connected diseases
No signs/symptoms info
Disease Type of connection
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Acute promyelocytic leukemia
Acute biphenotypic leukemia
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
Minimally differentiated acute myeloblastic leukemia
Familial pancreatic carcinoma
Amyotrophic lateral sclerosis
Young adult-onset Parkinsonism
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Hereditary breast and ovarian cancer syndrome
Juvenile myelomonocytic leukemia
Autosomal agammaglobulinemia
SHORT syndrome
Behavioral variant of frontotemporal dementia
Fanconi anemia
Progressive non-fluent aphasia
Semantic dementia
Inflammatory myofibroblastic tumor
Retinitis pigmentosa
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Anaplastic ependymoma
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
Primary peritoneal carcinoma
Cowden syndrome
Ear-patella-short stature syndrome
Proteus syndrome
12q14 microdeletion syndrome
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
46,XY complete gonadal dysgenesis
Fibronectin glomerulopathy
LEOPARD syndrome
Noonan syndrome
Multiple endocrine neoplasia type 1
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Ewing sarcoma
Extraskeletal Ewing sarcoma
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Peripheral primitive neuroectodermal tumor
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Cone rod dystrophy
Primary ciliary dyskinesia
Primary ciliary dyskinesia - retinitis pigmentosa
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
Chronic mucocutaneous candidiasis
Coffin-Siris syndrome
Combined oxidative phosphorylation defect type 4
Common variable immunodeficiency
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
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
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
Translocation renal cell carcinoma
Unilateral retinoblastoma
X-linked Opitz G / BBB 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
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
PLCG2-associated antibody deficiency and immune dysregulation
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Glycogen storage disease due to LAMP-2 deficiency
(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: D015479

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