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Papillary or follicular thyroid carcinoma
3 OMIM references -
16 associated genes
294 connected diseases
No signs/symptoms info
Disease Type of connection
Thyroid hypoplasia
Familial medullary thyroid carcinoma
Extraskeletal myxoid chondrosarcoma
Hirschsprung disease
Hereditary sensory and autonomic neuropathy type 5
Bamforth syndrome
Benign familial chorea
Bilateral renal agenesis
Bilateral renal dysplasia
Brain-lung-thyroid syndrome
Distal monosomy 12p
Familial renal cell carcinoma
Haddad syndrome
Hereditary motor and sensory neuropathy, Okinawa type
Hereditary sensory and autonomic neuropathy type 4
Multiple endocrine neoplasia type 2A
Multiple endocrine neoplasia type 2B
Spastic paraplegia-optic atrophy-neuropathy syndrome
Unilateral renal dysplasia
Acute promyelocytic leukemia
Bardet-Biedl syndrome
Precursor T-cell acute lymphoblastic leukemia
Precursor B-cell acute lymphoblastic leukemia
Giant cell glioblastoma
Familial pancreatic carcinoma
Autosomal agammaglobulinemia
Juvenile myelomonocytic leukemia
Amyotrophic lateral sclerosis
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Translocation renal cell carcinoma
Chronic myeloid leukemia
Essential thrombocythemia
Hypohidrotic ectodermal dysplasia with immunodeficiency
SHORT syndrome
Young adult-onset Parkinsonism
Glucocorticoid resistance
Coffin-Siris syndrome
Cornelia de Lange syndrome
Pseudohypoaldosteronism type 2E
Autosomal dominant hyper-IgE syndrome
Distal 22q11.2 microdeletion syndrome
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Estrogen resistance syndrome
Noonan syndrome
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Familial partial lipodystrophy associated with PPARG mutations
Autosomal dominant hypohidrotic ectodermal dysplasia
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Li-Fraumeni syndrome
Papilloma of choroid plexus
Huntington disease
Juvenile Huntington disease
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Autosomal dominant nonsyndromic intellectual deficit
Combined immunodeficiency due to STK4 deficiency
Melanoma of soft part
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Pediatric systemic lupus erythematosus
Herpetic encephalitis
Hypocalcemic vitamin D-resistant rickets
Autosomal dominant secondary polycythemia
Blackfan-Diamond anemia
Cabezas syndrome
Extraskeletal Ewing sarcoma
Inflammatory myofibroblastic tumor
Multiple paragangliomas associated with polycythemia
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Retinitis pigmentosa
Berardinelli-Seip congenital lipodystrophy
Left ventricular noncompaction
Meckel syndrome
Senior-Loken syndrome
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
LEOPARD syndrome
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Pseudohyperaldosteronism type 2
Renal pseudohypoaldosteronism type 1
Distal 16p11.2 microdeletion syndrome
Proximal 16p11.2 microdeletion syndrome
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
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
Myelofibrosis with myeloid metaplasia
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
Generalized congenital lipodystrophy with myopathy
Peripheral resistance to thyroid hormones
Familial retinoblastoma
Microcephalic osteodysplastic primordial dwarfism type 2
Monosomy 13q14
Seckel syndrome
Unilateral retinoblastoma
Anaplastic ependymoma
Autosomal recessive limb-girdle muscular dystrophy type 2H
Cerebellar ataxia-deafness-narcolepsy syndrome
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Mucolipidosis type 4
Acute megakaryoblastic leukemia without Down syndrome
Atrial septal defect, ostium secundum type
Burkitt lymphoma
Common variable immunodeficiency
Complete atrioventricular canal - ventricle hypoplasia
Congenital bilateral absence of vas deferens
Congenital diaphragmatic hernia
Cystic fibrosis
Familial atrial fibrillation
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Fibronectin glomerulopathy
Fuchs endothelial corneal dystrophy
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Isolated brachycephaly
Isolated delta-storage pool disease
Isolated plagiocephaly
Male infertility with normal virilization due to meiosis defect
Pallister-Hall syndrome
Pancreatic hypoplasia - diabetes - congenital heart disease
Peters anomaly
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Tetralogy of Fallot
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Angelman syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Giant cell arteritis
Granulomatosis with polyangiitis
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
T-B+ severe combined immunodeficiency due to CD45 deficiency
Cone rod dystrophy
APC-related attenuated familial adenomatous polyposis
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Alopecia universalis
Alveolar rhabdomyosarcoma
Anophthalmia / microphthalmia - esophageal atresia
Atrichia with papular lesions
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Autosomal dominant aplasia and myelodysplasia
Autosomal dominant limb-girdle muscular dystrophy type 1A
Autosomal recessive cerebellar ataxia with late-onset spasticity
Autosomal recessive spastic paraplegia type 30
Autosomal recessive spastic paraplegia type 46
Behçet disease
Blau syndrome
Colobomatous microphthalmia
Commissural facial cleft
Congenital dyserythropoietic anemia type II
Cowden syndrome
Cree leukoencephalopathy
Dent disease type 2
Desmoid tumor
Desmoplastic small round cell tumor
Ewing sarcoma
Familial adenomatous polyposis due to 5q22.2 microdeletion
Familial congenital palsy of trochlear nerve
Familial gastric cancer
Familial isolated dilated cardiomyopathy
Familial multiple meningioma
Familial prostate cancer
Familial rhabdoid tumor
Fatal infantile hypertonic myofibrillar myopathy
Feingold syndrome type 1
Frontotemporal dementia with motor neuron disease
Gardner syndrome
Gastric linitis plastica
Gray platelet syndrome
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary gingival fibromatosis
Hereditary nonpolyposis colon cancer
Hereditary sensory and autonomic neuropathy type 2
Hereditary site-specific ovarian cancer syndrome
Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies
Idiopathic pulmonary fibrosis
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Inherited congenital spastic tetraplegia
Intellectual deficit - sparse hair - brachydactyly
Intellectual deficit, X-linked, Nascimento type
Isolated anophthalmia - microphthalmia
Joubert syndrome with hepatic defect
Joubert syndrome with renal defect
Juvenile amyotrophic lateral sclerosis
Keratosis palmoplantaris striata
LIG4 syndrome
Laron syndrome with immunodeficiency
Lethal acantholytic epidermolysis bullosa
Majeed syndrome
Marie Unna hereditary hypotrichosis
Microcephalic primordial dwarfism, Dauber type
Monomelic amyotrophy
Mosaic variegated aneuploidy syndrome
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
Myotilin-related myofibrillar myopathy without spheroid body
Myxoid / round cell liposarcoma
Nuclear cataract
Oculocerebrorenal syndrome
Omenn syndrome
Pontocerebellar hypoplasia type 1
Posterior polar cataract
Primary peritoneal carcinoma
Proteus syndrome
Septo-optic dysplasia
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Solitary fibrous tumor
Spheroid body myopathy
Spinocerebellar ataxia type 1 with axonal neuropathy
Spinocerebellar ataxia type 2
Spinocerebellar ataxia type 7
Split hand-split foot malformation
Tessier number 4 facial cleft
Transaldolase deficiency
Turcot syndrome with polyposis
Williams syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
X-linked intellectual deficit, Najm type
X-linked lymphoproliferative disease
Zonular cataract
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
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
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Hyperinsulinism due to HNF4A deficiency
Joubert syndrome with oculorenal defect
Leber congenital amaurosis
MODY syndrome
Ondine syndrome
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Costello syndrome
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Lethal restrictive dermopathy
Linear nevus sebaceus syndrome
Mandibuloacral dysplasia with type A lipodystrophy
Mandibulofacial dysostosis-microcephaly syndrome
Phakomatosis pigmentokeratotica
Progeria-associated arthropathy
Severe combined immunodeficiency due to DNA-PKcs deficiency
- Well-differentiated thyroid carcinoma

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

Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.