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Familial pancreatic carcinoma
5 OMIM references -
8 associated genes
530 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary breast and ovarian cancer syndrome
Fanconi anemia
Familial prostate cancer
Precursor B-cell acute lymphoblastic leukemia
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Precursor T-cell acute lymphoblastic leukemia
B-cell chronic lymphocytic leukemia
Hereditary nonpolyposis colon cancer
Li-Fraumeni syndrome
Giant cell glioblastoma
Familial melanoma
Primary peritoneal carcinoma
Essential thrombocythemia
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Adrenocortical carcinoma
Papilloma of choroid plexus
Noonan syndrome
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Juvenile myelomonocytic leukemia
Pilocytic astrocytoma
Costello syndrome
Linear nevus sebaceus syndrome
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Cardiofaciocutaneous syndrome
Blackfan-Diamond anemia
Amyotrophic lateral sclerosis
Split hand-split foot malformation
Familial thoracic aortic aneurysm and aortic dissection
Seckel syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Constitutional mismatch repair deficiency syndrome
Non-polyposis Turcot syndrome
Coffin-Siris syndrome
Familial isolated dilated cardiomyopathy
Mantle cell lymphoma
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Muir-Torre syndrome
Acute promyelocytic leukemia
Familial rhabdoid tumor
Young adult-onset Parkinsonism
Melanoma of soft part
Familial congenital mirror movements
Distal 22q11.2 microdeletion syndrome
Cowden syndrome
Aneurysm - osteoarthritis syndrome
Chronic myeloid leukemia
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
46,XY partial gonadal dysgenesis
Papillary or follicular thyroid carcinoma
Retinitis pigmentosa
Baraitser-Winter syndrome
Multiple endocrine neoplasia type 1
Proteus syndrome
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Ataxia-telangiectasia variant
Combined cervical dystonia
Osteogenesis imperfecta type 3
Estrogen resistance syndrome
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
3M syndrome
COFS syndrome
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Burkitt lymphoma
Angelman syndrome
Follicular lymphoma
Intravascular large B-cell lymphoma
Squamous cell carcinoma of head and neck
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Intellectual deficit, X-linked, Turner type
Autosomal recessive primary microcephaly
Familial advanced sleep-phase syndrome
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Bladder exstrophy
Desmoplastic small round cell tumor
EEC syndrome
Limb-mammary syndrome
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
UV-sensitive syndrome
Williams syndrome
Cerebellar ataxia - hypogonadism
Ewing sarcoma
Extraskeletal Ewing sarcoma
Autosomal dominant nonsyndromic intellectual deficit
Xeroderma pigmentosum variant
Leber hereditary optic neuropathy
MELAS syndrome
Maternally-inherited Leigh syndrome
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Cornelia de Lange syndrome
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Intermediate nemaline myopathy
Multiple myeloma
Intellectual deficit, X-linked, Nascimento type
Adult-onset distal myopathy due to VCP mutation
Behavioral variant of frontotemporal dementia
Familial retinoblastoma
Monosomy 13q14
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
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Unilateral retinoblastoma
Chuvash erythrocytosis
Von Hippel-Lindau disease
Werner syndrome
Spinocerebellar ataxia type 26
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
1p36 deletion syndrome
Branchio-oculo-facial syndrome
Jawad syndrome
Shprintzen-Goldberg syndrome
Anaplastic ependymoma
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
Pontocerebellar hypoplasia type 1
Terminal osseous dysplasia - pigmentary defects
Lennox-Gastaut syndrome
Severe combined immunodeficiency due to DNA-PKcs deficiency
Autosomal dominant progressive external ophthalmoplegia
Developmental delay with autism spectrum disorder and gait instability
WAGR syndrome
Hereditary spherocytosis
Hyperinsulinism due to HNF4A deficiency
MODY syndrome
Bloom syndrome
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
Atypical teratoid tumor
Familial multiple meningioma
Neurofibromatosis type 3
Myelodysplastic syndromes
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
17q11 microdeletion syndrome
Ear-patella-short stature syndrome
Heritable pulmonary arterial hypertension
Hypocalcemic vitamin D-resistant rickets
Extraskeletal myxoid chondrosarcoma
Fatal infantile hypertonic myofibrillar myopathy
Fibronectin glomerulopathy
Posterior polar cataract
Zonular cataract
Developmental malformations - deafness - dystonia
Lissencephaly due to TUBA1A mutation
Loeys-Dietz syndrome type 1
46,XY complete gonadal dysgenesis
Glycogen storage disease due to liver phosphorylase kinase deficiency
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Peters anomaly
Zellweger syndrome
Common variable immunodeficiency
Autoimmune lymphoproliferative syndrome
Congenital myopathy with excess of thin filaments
Familial isolated congenital asplenia
Inflammatory myofibroblastic tumor
Severe congenital nemaline myopathy
Typical nemaline myopathy
LEOPARD syndrome
Hypohidrotic ectodermal dysplasia with immunodeficiency
Ataxia-telangiectasia-like disorder
Huntington disease
Juvenile Huntington disease
Nijmegen breakage syndrome-like disorder
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Spinocerebellar ataxia type 17
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
BAP1-related tumor predisposition syndrome
Chronic mucocutaneous candidiasis
Dystonia 16
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Xeroderma pigmentosum complementation group B
Autosomal recessive cutis laxa type 1
Isolated brachycephaly
Isolated scaphocephaly
Lethal arteriopathy syndrome due to FBLN4 deficiency
Saethre-Chotzen syndrome
Xeroderma pigmentosum complementation group D
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Bannayan-Riley-Ruvalcaba syndrome
Distal hereditary motor neuropathy type 2
Glucocorticoid resistance
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Juvenile polyposis of infancy
Kearns-Sayre syndrome
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Mitochondrial neurogastrointestinal encephalomyopathy
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
17p13.3 microduplication syndrome
Acute myeloid leukemia
Budd-Chiari syndrome
Catecholaminergic polymorphic ventricular tachycardia
Deafness - lymphedema - leukemia
Denys-Drash syndrome
Distal 17p13.3 microdeletion syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial thrombocytosis
Frasier syndrome
Meacham syndrome
Miller-Dieker syndrome
Monocytopenia with susceptibility to infections
Myelofibrosis with myeloid metaplasia
Peutz-Jeghers syndrome
Polycythemia vera
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Alveolar soft-part sarcoma
Hereditary pheochromocytoma-paraganglioma
Translocation renal cell carcinoma
X-linked distal arthrogryposis multiplex congenita
Joubert syndrome with oculorenal defect
Nijmegen breakage syndrome
Noonan syndrome-like disorder with loose anagen hair
X-linked dystonia-parkinsonism
Generalized resistance to thyroid hormone
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
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Left ventricular noncompaction
Ataxia - oculomotor apraxia type 1
Alobar holoprosencephaly
Autosomal agammaglobulinemia
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Mosaic variegated aneuploidy syndrome
Multiple keratoacanthoma, Ferguson-Smith type
SHORT syndrome
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Atypical Gaucher disease due to saposin C deficiency
Encephalopathy due to prosaposin deficiency
Infantile Krabbe disease
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Constitutional megaloblastic anemia with severe neurologic disease
Inherited acute myeloid leukemia
Isolated delta-storage pool disease
Paris-Trousseau thrombocytopenia
Paternal uniparental disomy of chromosome 6
Peripheral primitive neuroectodermal tumor
Premature chromosome condensation with microcephaly and intellectual deficit
Transient neonatal diabetes mellitus
Weaver syndrome
Alveolar rhabdomyosarcoma
Familial drusen
Autosomal dominant distal renal tubular acidosis
Cerebellar ataxia-deafness-narcolepsy syndrome
Congenital lactic acidosis, Saguenay-Lac-St. Jean type
Distal renal tubular acidosis with anemia
Intellectual deficit - sparse hair - brachydactyly
Keratosis follicularis spinulosa decalvans
Prader-Willi syndrome due to translocation
Primary CD59 deficiency
Purine nucleoside phosphorylase deficiency
Southeast Asian ovalocytosis
Synpolydactyly type 2
Young adult-onset distal hereditary motor neuropathy
Autosomal recessive nonsyndromic intellectual deficit
Cone rod dystrophy
Congenital analbuminemia
Endocrine-cerebro-osteodysplasia syndrome
Ethylmalonic encephalopathy
Leber congenital amaurosis
MMEP syndrome
Meckel syndrome
Wilson-Turner syndrome
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
CLOVE syndrome
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
17q11.2 microduplication syndrome
MACS syndrome
Methylcobalamin deficiency type cblG
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion
Reducing body myopathy
Spondylo-megaepiphyseal-metaphyseal dysplasia
Watson syndrome
X-linked Emery-Dreifuss muscular dystrophy
X-linked lymphoproliferative disease
X-linked myopathy with postural muscle atrophy
Omenn syndrome
Severe combined immunodeficiency due to DCLRE1C deficiency
Combined immunodeficiency due to STK4 deficiency
Cabezas syndrome
Hypodontia - dysplasia of nails
Male infertility with normal virilization due to meiosis defect
Systemic-onset juvenile idiopathic arthritis
22q11.2 deletion syndrome
Alpha-1-antitrypsin deficiency
Alpha-thalassemia - X-linked intellectual deficit syndrome
Alpha-thalassemia - myelodysplastic syndrome
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Aniridia - cerebellar ataxia - intellectual deficit
Atrial septal defect - atrioventricular conduction defects
Atrial septal defect, ostium secundum type
Autoimmune lymphoproliferative syndrome with recurrent infections
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal dominant keratitis
Autosomal dominant limb-girdle muscular dystrophy type 1D
Autosomal dominant secondary polycythemia
Autosomal dominant severe congenital neutropenia
Autosomal recessive limb-girdle muscular dystrophy type 2O
Autosomal recessive limb-girdle muscular dystrophy type 2S
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal recessive spastic paraplegia type 45
Autosomal recessive systemic lupus erythematosus
Autosomal thrombocytopenia with normal platelets
Caffey disease
Cap myopathy
Carpenter-Waziri syndrome
Chudley-Lowry-Hoar syndrome
Cleidocranial dysplasia
Colobomatous microphthalmia
Congenital communicating hydrocephalus
Congenital fibrosis of extraocular muscles
Congenital muscular dystrophy with cerebellar involvement
Congenital stromal corneal dystrophy
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Dermatofibrosarcoma protuberans
Distal 16p11.2 microdeletion syndrome
Distal monosomy 3p
Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, vascular-like type
Ehlers-Danlos / osteogenesis imperfecta syndrome
FTH1-related iron overload
Familial atrial fibrillation
Familial cortical myoclonus
Familial progressive cardiac conduction defect
Fatal infantile cytochrome C oxidase deficiency
Feingold syndrome type 1
Foveal hypoplasia - presenile cataract
Frontotemporal dementia with motor neuron disease
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
Gray platelet syndrome
Growth delay due to insulin-like growth factor I resistance
Gräsbeck-Imerslund disease
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
High bone mass osteogenesis imperfecta
Holmes-Gang syndrome
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
Hypoparathyroidism - deafness - renal disease
Hypoplastic left heart syndrome
Hypotrichosis simplex
Infantile onset spinocerebellar ataxia
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
Isolated ATP synthase deficiency
Isolated aniridia
Isolated optic nerve hypoplasia
Juberg-Marsidi syndrome
Leber 'plus' disease
Leigh syndrome with cardiomyopathy
Lethal acantholytic epidermolysis bullosa
Ligneous conjunctivitis
Male infertility associated with large-headed multiflagellar polyploid spermatozoa
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty
Mitochondrial DNA depletion syndrome, hepatocerebrorenal form
Mitochondrial nonsyndromic sensorineural deafness with susceptibility to aminoglycoside exposure
Morning glory syndrome
Moyamoya disease
Muscle-eye-brain disease
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Naxos disease
Niemann-Pick disease type C, adult neurologic onset
Niemann-Pick disease type C, juvenile neurologic onset
Niemann-Pick disease type C, late infantile neurologic onset
Niemann-Pick disease type C, severe early infantile neurologic onset
Niemann-Pick disease type C, severe perinatal form
Osteogenesis imperfecta type 1
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 4
Phakomatosis pigmentokeratotica
Pontocerebellar hypoplasia type 2
Pontocerebellar hypoplasia type 4
Pontocerebellar hypoplasia type 5
Proximal 16p11.2 microdeletion syndrome
Rare isolated myopia
Renal coloboma syndrome
Renal tubular dysgenesis of genetic origin
Richieri Costa-Pereira syndrome
Schimke immuno-osseous dysplasia
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
Single ventricular septal defect
Smith-Fineman-Myers syndrome
Smith-Magenis syndrome
Solitary fibrous tumor
Spinocerebellar ataxia type 18
Tetralogy of Fallot
Thyroid hypoplasia
Triose phosphate-isomerase deficiency
Usher syndrome type 2
Waardenburg syndrome type 2
Walker-Warburg syndrome
X-linked non-syndromic intellectual deficit
Xeroderma pigmentosum complementation group C
Autosomal dominant hyper-IgE syndrome
Familial capillary hemangioma
GAPO syndrome
Kleefstra syndrome due to 9q34 microdeletion
Kleefstra syndrome due to a point mutation
Early-onset autosomal dominant Alzheimer disease
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Focal facial dermal dysplasia
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
Romano-Ward syndrome
Zollinger-Ellison syndrome
14q11.2 microduplication syndrome
14q12 microdeletion syndrome
17q21.31 microdeletion syndrome
Acrocallosal syndrome
Acute necrotizing encephalopathy of childhood
Atypical Rett syndrome
Autosomal recessive lymphoproliferative disease
Berardinelli-Seip congenital lipodystrophy
Congenital intrauterine infection-like syndrome
Diffuse cutaneous systemic sclerosis
Familial acute necrotizing encephalopathy
Greig cephalopolysyndactyly syndrome
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
Koolen-De Vries syndrome due to a point mutation
Large congenital melanocytic nevus
Limited cutaneous systemic sclerosis
Marfan syndrome type 2
Neutrophil immunodeficiency syndrome
Pallister-Hall syndrome
Polysyndactyly, bilateral
Polysyndactyly, unilateral
Postaxial polydactyly type A, bilateral
Postaxial polydactyly type A, unilateral
Postaxial polydactyly type B, bilateral
Postaxial polydactyly type B, unilateral
Pulmonary capillary hemangiomatosis
Pulmonary venoocclusive disease
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Spinocerebellar ataxia type 12
X-linked agammaglobulinemia
X-linked hyper-IgM 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
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
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Progeria-associated arthropathy
- Familial pancreatic cancer

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

Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
External references:
5 OMIM references -
1 MeSH reference: C535837

No signs/symptoms info available.