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Precursor B-cell acute lymphoblastic leukemia
1 OMIM reference -
20 associated genes
586 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor T-cell acute lymphoblastic leukemia
Chronic myeloid leukemia
Familial pancreatic carcinoma
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute biphenotypic leukemia
MALT lymphoma
Distal 22q11.2 microdeletion syndrome
B-cell chronic lymphocytic leukemia
Giant cell glioblastoma
Acute myeloblastic leukemia with maturation
Essential thrombocythemia
Autosomal agammaglobulinemia
Li-Fraumeni syndrome
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Mantle cell lymphoma
Adrenocortical carcinoma
Papilloma of choroid plexus
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Familial melanoma
Gastrointestinal stromal tumor
Isolated delta-storage pool disease
Chronic myelomonocytic leukemia
Idiopathic hypereosinophilic syndrome
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Follicular lymphoma
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Acute myeloid leukemia with 11q23 abnormalities
Acute undifferentiated leukemia
Autism spectrum disorder due to AUTS2 deficiency
Bilineal acute leukemia
Congenital mesoblastic nephroma
Hypoparathyroidism - deafness - renal disease
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Minimally differentiated acute myeloblastic leukemia
Myeloid neoplasm associated with PDGFRA rearrangement
Pancytopenia due to IKZF1 mutations
Wiedemann-Steiner syndrome
Hereditary breast and ovarian cancer syndrome
Blackfan-Diamond anemia
Coffin-Siris syndrome
Familial prostate cancer
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute promyelocytic leukemia
Amyotrophic lateral sclerosis
Familial rhabdoid tumor
Young adult-onset Parkinsonism
Juvenile myelomonocytic leukemia
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Papillary or follicular thyroid carcinoma
Burkitt lymphoma
Noonan syndrome
Multiple endocrine neoplasia type 1
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Isolated brachycephaly
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
3M syndrome
Primary peritoneal carcinoma
Common variable immunodeficiency
Familial multiple meningioma
Seckel syndrome
Squamous cell carcinoma of head and neck
MODY syndrome
SHORT syndrome
Familial thoracic aortic aneurysm and aortic dissection
Congenital fiber-type disproportion myopathy
Familial isolated dilated cardiomyopathy
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Peters anomaly
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Acute basophilic leukemia
Cerebellar ataxia - hypogonadism
Spinocerebellar ataxia type 17
Bilateral striopallidodentate calcinosis
46,XY partial gonadal dysgenesis
Split hand-split foot malformation
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Hypocalcemic vitamin D-resistant rickets
Hypohidrotic ectodermal dysplasia with immunodeficiency
Berardinelli-Seip congenital lipodystrophy
Melanoma of soft part
Autosomal dominant nonsyndromic intellectual deficit
Autosomal recessive primary microcephaly
Childhood-onset nemaline myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Retinitis pigmentosa
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
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
Intellectual deficit, X-linked, Turner type
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Infantile myofibromatosis
Autosomal dominant progressive external ophthalmoplegia
Baraitser-Winter syndrome
Cerebellar ataxia-deafness-narcolepsy syndrome
Extraskeletal myxoid chondrosarcoma
Ear-patella-short stature syndrome
Heritable pulmonary arterial hypertension
Hereditary nonpolyposis colon cancer
Osteogenesis imperfecta type 3
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Anophthalmia / microphthalmia - esophageal atresia
Autosomal dominant spastic paraplegia type 13
Colobomatous microphthalmia
Isolated anophthalmia - microphthalmia
LEOPARD syndrome
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Septo-optic dysplasia
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Familial congenital mirror movements
Isolated scaphocephaly
Saethre-Chotzen syndrome
X-linked agammaglobulinemia
Ataxia-telangiectasia variant
Combined cervical dystonia
COFS syndrome
Xeroderma pigmentosum complementation group B
Aneurysm - osteoarthritis syndrome
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Intellectual deficit, X-linked, Nascimento type
Severe combined immunodeficiency due to DNA-PKcs deficiency
Angelman syndrome
Familial advanced sleep-phase syndrome
Prader-Willi syndrome due to imprinting mutation
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
Chuvash erythrocytosis
Von Hippel-Lindau disease
Werner syndrome
Acute megakaryoblastic leukemia without Down syndrome
Glucocorticoid resistance
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Bladder exstrophy
EEC syndrome
Limb-mammary syndrome
Spinocerebellar ataxia type 26
Hereditary gingival fibromatosis
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
Myeloid neoplasm associated with PDGFRB rearrangement
UV-sensitive syndrome
Unclassified chronic myeloproliferative disease
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Fanconi anemia
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Atypical teratoid tumor
Hereditary spherocytosis
Lennox-Gastaut syndrome
Neurofibromatosis type 3
Bannayan-Riley-Ruvalcaba syndrome
Cowden syndrome
Juvenile polyposis of infancy
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Proteus syndrome
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Desmoplastic small round cell tumor
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
Isolated plagiocephaly
Ewing sarcoma
Extraskeletal Ewing sarcoma
Diffuse cutaneous systemic sclerosis
Limited cutaneous systemic sclerosis
Uveal coloboma - cleft lip and palate - intellectual deficit
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
WAGR syndrome
Constitutional mismatch repair deficiency syndrome
Muir-Torre syndrome
Multiple myeloma
Non-polyposis Turcot syndrome
2q37 microdeletion syndrome
Alobar holoprosencephaly
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Budd-Chiari syndrome
Combined immunodeficiency due to STK4 deficiency
Developmental malformations - deafness - dystonia
Familial thrombocytosis
Lissencephaly due to TUBA1A mutation
Romano-Ward syndrome
Williams syndrome
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Autoimmune lymphoproliferative syndrome
Autosomal dominant centronuclear myopathy
Autosomal recessive systemic lupus erythematosus
Cone rod dystrophy
Distal myopathy with posterior leg and anterior hand involvement
Glycogen storage disease due to liver phosphorylase kinase deficiency
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Muscle filaminopathy
Autosomal dominant hypohidrotic ectodermal dysplasia
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Zollinger-Ellison syndrome
Athabaskan brainstem dysgenesis syndrome
Bosley-Salih-Alorainy syndrome
Myxoid / round cell liposarcoma
Partial pancreatic agenesis
Permanent neonatal diabetes mellitus
Inflammatory myofibroblastic tumor
Bloom syndrome
Branchio-oculo-facial syndrome
Dermatofibrosarcoma protuberans
Huntington disease
Juvenile Huntington disease
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Congenital hereditary facial paralysis with variable hearing loss
Dystonia 16
Familial medullary thyroid carcinoma
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Pontocerebellar hypoplasia type 1
Autosomal recessive cutis laxa type 1
Estrogen resistance syndrome
Lethal arteriopathy syndrome due to FBLN4 deficiency
Xeroderma pigmentosum complementation group D
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Kearns-Sayre syndrome
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Mitochondrial neurogastrointestinal encephalomyopathy
Denys-Drash syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Frasier syndrome
Intravascular large B-cell lymphoma
Meacham syndrome
Peutz-Jeghers syndrome
Pyogenic arthritis - pyoderma gangrenosum - acne
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Hyperinsulinism due to HNF4A deficiency
Developmental delay with autism spectrum disorder and gait instability
X-linked dystonia-parkinsonism
Congenital bilateral absence of vas deferens
Cystic fibrosis
Generalized resistance to thyroid hormone
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Peripheral resistance to thyroid hormones
Selective pituitary resistance to thyroid hormone
Hypotonia with lactic acidemia and hyperammonemia
Syndromic multisystem autoimmune disease due to Itch deficiency
7q31 microdeletion syndrome
Childhood apraxia of speech
Ataxia - oculomotor apraxia type 1
Paris-Trousseau thrombocytopenia
Peripheral primitive neuroectodermal tumor
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
Axenfeld anomaly
Axenfeld-Rieger syndrome
Catecholaminergic polymorphic ventricular tachycardia
Rieger anomaly
Autosomal dominant limb-girdle muscular dystrophy type 1C
Constitutional megaloblastic anemia with severe neurologic disease
Paternal uniparental disomy of chromosome 6
Rippling muscle disease
Transient neonatal diabetes mellitus
Autosomal dominant macrothrombocytopenia
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
Adult-onset distal myopathy due to VCP mutation
Autosomal dominant distal renal tubular acidosis
Autosomal recessive nonsyndromic intellectual deficit
Combined immunodeficiency due to ZAP70 deficiency
Congenital lactic acidosis, Saguenay-Lac-St. Jean type
Distal monosomy 3p
Distal renal tubular acidosis with anemia
Fatal infantile hypertonic myofibrillar myopathy
Keratosis follicularis spinulosa decalvans
Posterior polar cataract
Prader-Willi syndrome due to translocation
Purine nucleoside phosphorylase deficiency
Southeast Asian ovalocytosis
Spastic paraplegia - Paget disease of bone
Zonular cataract
Cornelia de Lange syndrome
Endocrine-cerebro-osteodysplasia syndrome
Ethylmalonic encephalopathy
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
Wilson-Turner syndrome
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Charcot-Marie-Tooth disease type 2B2
Haddad syndrome
Incontinentia pigmenti
Leukocyte adhesion deficiency type I
MACS syndrome
Methylcobalamin deficiency type cblG
Ondine syndrome
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
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
Acute myeloid leukemia with CEBPA somatic mutations
Cabezas syndrome
Classical progressive supranuclear palsy
Congenital diaphragmatic hernia
Hypodontia - dysplasia of nails
Inherited acute myeloid leukemia
Progressive supranuclear palsy - corticobasal syndrome
Progressive supranuclear palsy - parkinsonism
Progressive supranuclear palsy - progressive non fluent aphasia
Progressive supranuclear palsy - pure akinesia with gait freezing
Systemic-onset juvenile idiopathic arthritis
Tetralogy of Fallot
16q24.3 microdeletion syndrome
1p36 deletion syndrome
22q11.2 deletion syndrome
46,XY complete gonadal dysgenesis
5q35 microduplication syndrome
ALDH18A1-related De Barsy syndrome
Acquired idiopathic sideroblastic anemia
Acrodysostosis with multiple hormone resistance
Acute myeloid leukemia
Acute myeloid leukemia with multilineage dysplasia
Alpha-1-antitrypsin deficiency
Alpha-thalassemia - X-linked intellectual deficit syndrome
Alpha-thalassemia - myelodysplastic syndrome
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis
Alveolar rhabdomyosarcoma
Anaplastic ependymoma
Atelosteogenesis type I
Atelosteogenesis type III
Atypical Rett syndrome
Autoimmune lymphoproliferative syndrome with recurrent infections
Autoimmune polyendocrinopathy type 1
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant Larsen syndrome
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant limb-girdle muscular dystrophy type 1D
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Autosomal dominant severe congenital neutropenia
Autosomal recessive limb-girdle muscular dystrophy type 2S
Autosomal recessive spastic paraplegia type 18
Autosomal recessive spastic paraplegia type 45
Beckwith-Wiedemann syndrome due to NSD1 mutation
Benign familial chorea
Beta-thalassemia - X-linked thrombocytopenia
Blepharophimosis-intellectual deficit syndrome, SBBYS type
Boomerang dysplasia
Brain-lung-thyroid syndrome
Brugada syndrome
Carpenter-Waziri syndrome
Charcot-Marie-Tooth disease type 4F
Chronic intestinal pseudoobstruction
Chudley-Lowry-Hoar syndrome
Classic multiminicore myopathy
Cleidocranial dysplasia
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy
Congenital communicating hydrocephalus
Congenital erythropoietic porphyria
Congenital fibrosis of extraocular muscles
Congenital glaucoma
Congenital short bowel syndrome
Congenital stationary night blindness
Congenital valvular dysplasia
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Costello syndrome
Craniofacial-deafness-hand syndrome
Deafness - lymphedema - leukemia
Dejerine-Sottas syndrome
Desmin-related myopathy with Mallory body-like inclusions
Donnai-Barrow syndrome
Ehlers-Danlos syndrome with periventricular heterotopia
Exfoliative ichthyosis
FTH1-related iron overload
Familial cortical myoclonus
Familial sick sinus syndrome
Fatal infantile cytochrome C oxidase deficiency
Feingold syndrome type 1
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Fibronectin glomerulopathy
Frontometaphyseal dysplasia
Frontotemporal dementia with motor neuron disease
Fuchs endothelial corneal dystrophy
Genitopatellar syndrome
Glaucoma secondary to spherophakia / ectopia lentis and megalocornea
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
Greenberg dysplasia
Growth delay due to insulin-like growth factor I resistance
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Hereditary arterial and articular multiple calcification syndrome
Herpetic encephalitis
Holmes-Gang syndrome
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
Hypotrichosis simplex
Idiopathic CD4 lymphocytopenia
Immunodeficiency due to a late component of complements deficiency
Infantile Refsum disease
Infantile autosomal recessive medullary cystic kidney disease
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Infantile onset spinocerebellar ataxia
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Inherited congenital spastic tetraplegia
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
Isolated ATP synthase deficiency
Isolated CoQ-cytochrome C reductase deficiency
Jawad syndrome
Juberg-Marsidi syndrome
Juvenile amyotrophic lateral sclerosis
Juvenile primary lateral sclerosis
KBG syndrome
Leigh syndrome with cardiomyopathy
Leigh syndrome with nephrotic syndrome
Lethal congenital contracture syndrome type 2
Linear nevus sebaceus syndrome
Lissencephaly type 1 due to doublecortin gene mutation
Loeys-Dietz syndrome type 1
MMEP syndrome
Mandibular hypoplasia-deafness-progeroid syndrome
Marfan syndrome type 2
Matthew-Wood syndrome
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty
Microcephalic primordial dwarfism, Alazami type
Mitochondrial DNA depletion syndrome, hepatocerebrorenal form
Monocytopenia with susceptibility to infections
Monosomy 22q13
Moyamoya disease
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Myelodysplastic syndromes
Nager syndrome
Neonatal adrenoleukodystrophy
Obesity due to prohormone convertase I deficiency
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pallister-Hall syndrome
Periventricular nodular heterotopia
Phakomatosis pigmentokeratotica
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Rare isolated myopia
Recessive intellectual disability - motor dysfunction - multiple joint contractures
Refractory anemia
Refractory anemia with excess blasts
Renal tubular dysgenesis of genetic origin
Renal-hepatic-pancreatic dysplasia
Reynolds syndrome
Rigid spine syndrome
Sanfilippo syndrome type D
Schimke immuno-osseous dysplasia
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
Shprintzen-Goldberg syndrome
Smith-Fineman-Myers syndrome
Solitary fibrous tumor
Sotos syndrome
Spinocerebellar ataxia type 18
Spondylocarpotarsal synostosis
Spondylometaphyseal dysplasia - cone-rod dystrophy
Subcortical band heterotopia
Tay-Sachs disease, B variant, adult form
Tay-Sachs disease, B variant, infantile form
Tay-Sachs disease, B variant, juvenile form
Tay-Sachs disease, B1 variant
Terminal osseous dysplasia - pigmentary defects
Thrombocytopenia with congenital dyserythropoietic anemia
Thyroid hypoplasia
Triose phosphate-isomerase deficiency
Van den Ende-Gupta syndrome
Waardenburg syndrome type 1
Waardenburg syndrome type 2
Waardenburg syndrome type 3
Weaver syndrome
Weill-Marchesani syndrome
West syndrome
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
X-linked non-syndromic intellectual deficit
Xeroderma pigmentosum complementation group C
Zellweger syndrome
Kleefstra syndrome due to 9q34 microdeletion
Kleefstra syndrome due to a point mutation
Multiple endocrine neoplasia type 4
Focal facial dermal dysplasia
Hereditary pheochromocytoma-paraganglioma
Autosomal recessive centronuclear myopathy
Barth syndrome
Dyskeratosis congenita
Hoyeraal-Hreidarsson syndrome
Idiopathic aplastic anemia
Idiopathic pulmonary fibrosis
Left ventricular noncompaction
17q21.31 microdeletion syndrome
Acute necrotizing encephalopathy of childhood
Aniridia - cerebellar ataxia - intellectual deficit
Atypical hemolytic uremic syndrome with C3 anomaly
Autosomal dominant hyper-IgE syndrome
Autosomal dominant keratitis
Chronic mucocutaneous candidiasis
Complement component 3 deficiency
Congenital vertical talus, bilateral
Congenital vertical talus, unilateral
Familial acute necrotizing encephalopathy
Foveal hypoplasia - presenile cataract
Hyperinsulinism due to HNF1A deficiency
Isolated aniridia
Isolated optic nerve hypoplasia
Koolen-De Vries syndrome due to a point mutation
Laron syndrome with immunodeficiency
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Monosomy 5p
Morning glory syndrome
Nail-patella syndrome
Spinocerebellar ataxia type 12
Susceptibility to viral and mycobacterial infections
Translocation renal cell carcinoma
X-linked hyper-IgM syndrome
Xeroderma pigmentosum complementation group E
- Precursor B-cell acute lymphoblastic leukemia/lymphoma
- Precursor B-cell acute lymphocytic leukemia
- Precursor B-cell acute lymphocytic leukemia/lymphoma

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

Classification (ICD10):
- Neoplasms -

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

No signs/symptoms info available.