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Precursor T-cell acute lymphoblastic leukemia
20 associated genes
584 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor B-cell acute lymphoblastic leukemia
Chronic myeloid leukemia
Familial pancreatic carcinoma
Distal 22q11.2 microdeletion syndrome
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Familial melanoma
Acute myeloblastic leukemia with maturation
Autosomal recessive primary microcephaly
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Burkitt lymphoma
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute basophilic leukemia
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Acute biphenotypic leukemia
Minimally differentiated acute myeloblastic leukemia
B-cell chronic lymphocytic leukemia
Giant cell glioblastoma
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Hereditary breast and ovarian cancer syndrome
Young adult-onset Parkinsonism
Essential thrombocythemia
Papillary or follicular thyroid carcinoma
Amyotrophic lateral sclerosis
Common variable immunodeficiency
Noonan syndrome
Juvenile myelomonocytic leukemia
Retinitis pigmentosa
Familial prostate cancer
Baraitser-Winter syndrome
Acute promyelocytic leukemia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Adrenocortical carcinoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Fanconi anemia
Williams syndrome
Fibronectin glomerulopathy
Familial isolated dilated cardiomyopathy
Blackfan-Diamond anemia
Hereditary nonpolyposis colon cancer
Inflammatory myofibroblastic tumor
Coffin-Siris syndrome
Familial rhabdoid tumor
Autosomal dominant nonsyndromic intellectual deficit
Autosomal agammaglobulinemia
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Mantle cell lymphoma
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Isolated NADH-CoQ reductase deficiency
Translocation renal cell carcinoma
Hypohidrotic ectodermal dysplasia with immunodeficiency
Ear-patella-short stature syndrome
LEOPARD syndrome
Chuvash erythrocytosis
Von Hippel-Lindau disease
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Left ventricular noncompaction
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Constitutional mismatch repair deficiency syndrome
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Cerebellar ataxia - hypogonadism
Primary peritoneal carcinoma
Multiple endocrine neoplasia type 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Developmental malformations - deafness - dystonia
Congenital fiber-type disproportion myopathy
Ataxia-telangiectasia variant
Combined cervical dystonia
SHORT syndrome
Intellectual deficit, X-linked, Turner type
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Extraskeletal Ewing sarcoma
Autosomal recessive centronuclear myopathy
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Chronic intestinal pseudoobstruction
Congenital short bowel syndrome
Congenital valvular dysplasia
Ehlers-Danlos syndrome with periventricular heterotopia
Frontometaphyseal dysplasia
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Terminal osseous dysplasia - pigmentary defects
Autosomal dominant Emery-Dreifuss muscular dystrophy
Cornelia de Lange syndrome
Isolated adermatoglyphia
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant centronuclear myopathy
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Seckel syndrome
Extraskeletal myxoid chondrosarcoma
Isolated brachycephaly
Isolated plagiocephaly
Childhood-onset nemaline myopathy
Typical nemaline myopathy
Atypical teratoid tumor
Familial multiple meningioma
Neurofibromatosis type 3
Xeroderma pigmentosum complementation group B
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cutaneous mastocytoma
Gastrointestinal stromal tumor
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
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Hereditary gingival fibromatosis
Isolated delta-storage pool disease
Hereditary spherocytosis
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Melanoma of soft part
Hypoparathyroidism - deafness - renal disease
Severe combined immunodeficiency due to DNA-PKcs deficiency
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Lissencephaly due to TUBA1A mutation
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Leigh syndrome with leukodystrophy
Osteogenesis imperfecta type 3
Richieri Costa-Pereira syndrome
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Estrogen resistance syndrome
Mosaic variegated aneuploidy syndrome
X-linked non-syndromic intellectual deficit
Catecholaminergic polymorphic ventricular tachycardia
Isolated CoQ-cytochrome C reductase deficiency
Mandibular hypoplasia-deafness-progeroid syndrome
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Split hand-split foot malformation
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Budd-Chiari syndrome
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Ewing sarcoma
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Familial thrombocytosis
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
Intellectual deficit - sparse hair - brachydactyly
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Mitochondrial trifunctional protein deficiency
Myelofibrosis with myeloid metaplasia
Peripheral primitive neuroectodermal tumor
Polycythemia vera
Progeria-associated arthropathy
Zollinger-Ellison syndrome
17q11 microdeletion syndrome
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Capillary malformation - arteriovenous malformation
Follicular lymphoma
Parkes Weber syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1F
Bifunctional enzyme deficiency
Cabezas syndrome
Chronic mucocutaneous candidiasis
Cone rod dystrophy
Congenital stationary night blindness
Distal myopathy with posterior leg and anterior hand involvement
Frontotemporal dementia with motor neuron disease
Glycogen storage disease due to liver phosphorylase kinase deficiency
Muscle filaminopathy
Nager syndrome
Primary biliary cirrhosis
Pseudohypoaldosteronism type 2E
Spinocerebellar ataxia type 12
Acute necrotizing encephalopathy of childhood
Familial acute necrotizing encephalopathy
Generalized congenital lipodystrophy with myopathy
Congenital myopathy with excess of thin filaments
Idiopathic pulmonary fibrosis
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Weaver syndrome
Spinocerebellar ataxia type 26
Berardinelli-Seip congenital lipodystrophy
CLN2 disease
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
Omenn syndrome
Diffuse cutaneous systemic sclerosis
Limited cutaneous systemic sclerosis
MODY syndrome
Hereditary pheochromocytoma-paraganglioma
Fuchs endothelial corneal dystrophy
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Familial congenital mirror movements
Acute megakaryoblastic leukemia without Down syndrome
Beta-thalassemia - X-linked thrombocytopenia
Congenital erythropoietic porphyria
Thrombocytopenia with congenital dyserythropoietic anemia
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
Cowden syndrome
Proteus syndrome
Chorioretinopathy, Birdshot type
Familial medullary thyroid carcinoma
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Mandibulofacial dysostosis-microcephaly syndrome
Facial dysmorphism - immunodeficiency - livedo - short stature
Pilocytic astrocytoma
Congenital lactic acidosis, Saguenay-Lac-St. Jean type
Familial partial lipodystrophy due to AKT2 mutations
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Acute infantile liver failure-multisystemic involvement syndrome
Autosomal dominant optic atrophy plus syndrome
Autosomal dominant optic atrophy, classic type
Pyogenic arthritis - pyoderma gangrenosum - acne
Spinocerebellar ataxia type 17
Spinocerebellar ataxia type 36
Anaplastic ependymoma
Multiple myeloma
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Acrokeratosis verruciformis of Hopf
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Darier disease
Distal hereditary motor neuropathy type 2
Fatal infantile lactic acidosis with methylmalonic aciduria
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Branchio-oculo-facial syndrome
Cataract-microcornea syndrome
Cerulean cataract
Pulverulent cataract
Synovial sarcoma
Blepharophimosis-intellectual deficit syndrome, MKB type
FG syndrome type 1
Herpetic encephalitis
Intravascular large B-cell lymphoma
Recurrent infection due to specific granule deficiency
X-linked intellectual deficit with marfanoid habitus
Acute myeloid leukemia with CEBPA somatic mutations
Inherited acute myeloid leukemia
Autosomal dominant distal renal tubular acidosis
Charcot-Marie-Tooth disease type 4D
Combined immunodeficiency due to ZAP70 deficiency
Distal renal tubular acidosis with anemia
Intellectual deficit, X-linked, Nascimento type
Myxoid / round cell liposarcoma
Southeast Asian ovalocytosis
ALDH18A1-related De Barsy syndrome
Acute neonatal citrullinemia type I
Adams-Oliver syndrome
Adult-onset citrullinemia type I
Alobar holoprosencephaly
Atrial septal defect, ostium secundum type
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant limb-girdle muscular dystrophy type 1D
CLN1 disease
Citrullinemia type II
Complete androgen insensitivity syndrome
Congenital atransferrinemia
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
D,L-2-hydroxyglutaric aciduria
Distal monosomy 12p
Epileptic encephalopathy with global cerebral demyelination
Familial dysautonomia
Familial hypospadias
Familial vesicoureteral reflux
Fatal infantile cytochrome C oxidase deficiency
Glutaryl-CoA dehydrogenase deficiency
Gyrate atrophy of choroid and retina
Hereditary sensory and autonomic neuropathy type 1
Hyper-IgM syndrome type 3
Hypotonia with lactic acidemia and hyperammonemia
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Kennedy disease
Leigh syndrome with cardiomyopathy
Lobar holoprosencephaly
MALT lymphoma
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
Neonatal intrahepatic cholestasis due to citrin deficiency
Noonan syndrome-like disorder with loose anagen hair
Osteogenesis imperfecta type 2
Partial androgen insensitivity syndrome
Pediatric systemic lupus erythematosus
Proximal spinal muscular atrophy type 4
Rare isolated myopia
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Xanthinuria type I
Werner syndrome
1p36 deletion syndrome
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Bladder exstrophy
Charcot-Marie-Tooth disease type 2B2
EEC syndrome
Lennox-Gastaut syndrome
Leukocyte adhesion deficiency type I
Limb-mammary syndrome
MACS syndrome
Methylcobalamin deficiency type cblG
Shprintzen-Goldberg 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
Classical progressive supranuclear palsy
Combined immunodeficiency due to STK4 deficiency
Progressive supranuclear palsy - corticobasal syndrome
Progressive supranuclear palsy - parkinsonism
Progressive supranuclear palsy - progressive non fluent aphasia
Progressive supranuclear palsy - pure akinesia with gait freezing
22q11.2 deletion syndrome
3M syndrome
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
Acrodysostosis with multiple hormone resistance
Acute myeloid leukemia
Adult-onset distal myopathy due to VCP mutation
Alpers syndrome
Alveolar rhabdomyosarcoma
Amyotrophic lateral sclerosis type 4
Anophthalmia / microphthalmia - esophageal atresia
Atypical Rett syndrome
Autoimmune lymphoproliferative syndrome
Autoimmune polyendocrinopathy type 1
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Autosomal dominant progressive external ophthalmoplegia
Autosomal recessive ataxia, Beauce type
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive limb-girdle muscular dystrophy type 2J
Autosomal recessive myogenic arthrogryposis multiplex congenita
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal recessive progressive external ophthalmoplegia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Autosomal recessive spastic paraplegia type 56
Autosomal recessive systemic lupus erythematosus
Axenfeld anomaly
Axenfeld-Rieger syndrome
Behçet disease
Benign familial chorea
Borjeson-Forssman-Lehmann syndrome
Brain-lung-thyroid syndrome
Bruck syndrome
Brugada syndrome
Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
Cardiomyopathy - hypotonia - lactic acidosis
Charcot-Marie-Tooth disease type 4F
Charcot-Marie-Tooth disease type 4G
Chronic granulomatous disease
Chronic myelomonocytic leukemia
Classic multiminicore myopathy
Cleidocranial dysplasia
Colobomatous microphthalmia
Combined immunodeficiency T+ B+ due to partial RAG1 deficiency
Combined immunodeficiency with skin granulomas
Combined oxidative phosphorylation defect type 4
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy
Congenital fibrosis of extraocular muscles
Congenital glaucoma
Congenital mesoblastic nephroma
Congenital myasthenic syndromes with glycosylation defect
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Craniofacial-deafness-hand syndrome
Craniofrontonasal dysplasia
Deafness - lymphedema - leukemia
Dejerine-Sottas syndrome
Desmin-related myopathy with Mallory body-like inclusions
Distal hereditary motor neuropathy type 7
Distal monosomy 15q
Distal myopathy with vocal cord weakness
Donnai-Barrow syndrome
Early-onset myopathy with fatal cardiomyopathy
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
FASTKD2-related infantile mitochondrial encephalomyopathy
Familial atrial fibrillation
Familial sick sinus syndrome
Feingold syndrome type 1
Glaucoma secondary to spherophakia / ectopia lentis and megalocornea
Greenberg dysplasia
Griscelli disease type 1
Griscelli disease type 3
Hamel cerebro-palato-cardiac syndrome
Hereditary hypercarotenemia and vitamin A deficiency
Hereditary proximal myopathy with early respiratory failure
Hypocalcemic vitamin D-resistant rickets
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Idiopathic CD4 lymphocytopenia
Immunodeficiency due to a late component of complements deficiency
Immunodeficiency due to an early component of complement deficiency
Immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
Infantile Refsum disease
Infantile autosomal recessive medullary cystic kidney disease
Infantile myofibromatosis
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Inherited congenital spastic tetraplegia
Intermediate maple syrup urine disease
Isolated anophthalmia - microphthalmia
Isolated cytochrome C oxidase deficiency
Joubert syndrome
Keratosis palmoplantaris striata
Leigh syndrome with nephrotic syndrome
Lethal acantholytic epidermolysis bullosa
Lethal congenital contracture syndrome type 2
Leukocyte adhesion deficiency type III
Lymphedema - distichiasis
MMEP syndrome
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty
Mitochondrial neurogastrointestinal encephalomyopathy
Monocytopenia with susceptibility to infections
Monosomy 22q13
Mucopolysaccharidosis type 6, rapidly progressing
Mucopolysaccharidosis type 6, slowly progressing
Myelodysplastic syndromes
Neonatal adrenoleukodystrophy
Neuroectodermal melanolysosomal disease
Nijmegen breakage syndrome-like disorder
Non-spherocytic hemolytic anemia due to hexokinase deficiency
Occipital encephalocele
Perrault syndrome
Perry syndrome
Peters anomaly
Phosphoenolpyruvate carboxykinase 1 deficiency
Primary Fanconi syndrome
Primary ciliary dyskinesia
Quebec platelet disorder
Recessive mitochondrial ataxia syndrome
Renal-hepatic-pancreatic dysplasia
Reynolds syndrome
Rieger anomaly
Rigid spine syndrome
Ring dermoid of cornea
Sanfilippo syndrome type D
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Septo-optic dysplasia
Severe combined immunodeficiency due to complete RAG1 / 2 deficiency
Severe intellectual deficit and progressive spastic paraplegia
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia with axonal neuropathy type 2
Spinocerebellar ataxia with epilepsy
Squamous cell carcinoma of head and neck
Syndromic diarrhea
TARP syndrome
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
Thyroid hypoplasia
Tibial muscular dystrophy
Triose phosphate-isomerase deficiency
Van den Ende-Gupta syndrome
Waardenburg syndrome type 1
Waardenburg syndrome type 3
Weill-Marchesani syndrome
West syndrome
Wiskott-Aldrich syndrome
Wolf-Hirschhorn syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
X-linked distal arthrogryposis multiplex congenita
X-linked intellectual deficit - cerebellar hypoplasia
X-linked intellectual deficit, Golabi-Ito-Hall type
X-linked intellectual deficit, Porteous type
X-linked intellectual deficit, Sutherland-Haan type
X-linked sideroblastic anemia - ataxia
Zellweger syndrome
Multiple endocrine neoplasia type 4
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
Leber congenital amaurosis
Char syndrome
Dyskeratosis congenita
Hoyeraal-Hreidarsson syndrome
Idiopathic aplastic anemia
Polymicrogyria with optic nerve hypoplasia
Uveal coloboma - cleft lip and palate - intellectual deficit
Atypical hemolytic uremic syndrome with C3 anomaly
Autoimmune lymphoproliferative syndrome with recurrent infections
Bullous pemphigoid
Cardiofaciocutaneous syndrome
Combined immunodeficiency due to CD3gamma deficiency
Complement component 3 deficiency
Distal myopathy, Welander type
Familial infantile bilateral striatal necrosis
Heritable pulmonary arterial hypertension
Hyperinsulinism due to HNF1A deficiency
Juvenile rheumatoid factor-negative polyarthritis
Limited systemic sclerosis
Monosomy 5p
Narcolepsy without cataplexy
Oligoarticular juvenile arthritis
Xeroderma pigmentosum complementation group E
Acute fatty liver of pregnancy
Cap myopathy
Digitotalar dysmorphism
Dubin-Johnson syndrome
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Microphthalmia with linear skin defects syndrome
Oculopharyngeal muscular dystrophy
Romano-Ward syndrome
Sheldon-Hall syndrome
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
Trismus - pseudocamptodactyly
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
- Precursor T-cell acute lymphoblastic leukemia/lymphoma
- Precursor T-cell acute lymphocytic leukemia
- Precursor T-cell acute lymphocytic leukemia/lymphoma

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

Classification (ICD10):
- Neoplasms -

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

No signs/symptoms info available.