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Turcot syndrome with polyposis
1 OMIM reference -
1 associated gene
103 connected diseases
No signs/symptoms info
Disease Type of connection
Desmoid tumor
APC-related attenuated familial adenomatous polyposis
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Mosaic variegated aneuploidy syndrome
Autosomal dominant nonsyndromic intellectual deficit
Epidermolytic palmoplantar keratoderma
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Localized epidermolysis bullosa simplex
Retinitis pigmentosa
Young adult-onset Parkinsonism
Autosomal recessive epidermolysis bullosa simplex
Hepatocellular carcinoma, childhood-onset
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Lethal acantholytic epidermolysis bullosa
Naxos disease
Split hand-split foot malformation
Acute necrotizing encephalopathy of childhood
Familial acute necrotizing encephalopathy
Inflammatory myofibroblastic tumor
Branchio-oculo-facial syndrome
X-linked non-syndromic intellectual deficit
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Annular epidermolytic ichthyosis
Epidermolytic ichthyosis
Ichthyosis hystrix of Curth-Macklin
Keratosis palmoplantaris striata
2q23.1 microdeletion syndrome
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant macrothrombocytopenia
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal dominant secondary polycythemia
Autosomal recessive ataxia, Beauce type
Autosomal recessive myogenic arthrogryposis multiplex congenita
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Behçet disease
Childhood-onset nemaline myopathy
Chronic intestinal pseudoobstruction
Commissural facial cleft
Congenital bilateral absence of vas deferens
Congenital short bowel syndrome
Congenital valvular dysplasia
Cornelia de Lange syndrome
Cystic fibrosis
Dermatopathia pigmentosa reticularis
Dowling-Degos disease
Early infantile epileptic encephalopathy
Ehlers-Danlos syndrome with periventricular heterotopia
Epidermolysis bullosa simplex with circinate migratory erythema
Familial aortic dissection
Familial isolated dilated cardiomyopathy
Familial thoracic aortic aneurysm and aortic dissection
Frontometaphyseal dysplasia
Generalized junctional epidermolysis bullosa, non-Herlitz type
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Immunodeficiency due to an early component of complement deficiency
Intermediate nemaline myopathy
Junctional epidermolysis bullosa, Herlitz type
LOC syndrome
Leber 'plus' disease
Leber hereditary optic neuropathy
MELAS syndrome
Male infertility with normal virilization due to meiosis defect
Maternally-inherited Leigh syndrome
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Multiple paragangliomas associated with polycythemia
Naegeli-Franceschetti-Jadassohn syndrome
Oligodontia - cancer predisposition syndrome
Osteodysplasty, Melnick-Needles type
Osteopathia striata - cranial sclerosis
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pachyonychia congenita
Papillary or follicular thyroid carcinoma
Periventricular nodular heterotopia
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Severe congenital nemaline myopathy
Spectrin-associated autosomal recessive cerebellar ataxia
Spinocerebellar ataxia type 5
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Terminal osseous dysplasia - pigmentary defects
Tessier number 4 facial cleft
Typical nemaline myopathy
White sponge nevus
X-linked dystonia-parkinsonism
Craniolenticulosutural dysplasia
Hereditary sensory and autonomic neuropathy type 6
(no synonyms)

Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -

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

Gene symbol UniProt reference OMIM reference
APC P25054611731
No signs/symptoms info available.