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Familial prostate cancer
19 OMIM references -
12 associated genes
317 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary breast and ovarian cancer syndrome
Familial pancreatic carcinoma
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Fanconi anemia
Li-Fraumeni syndrome
Primary peritoneal carcinoma
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Nijmegen breakage syndrome
17q12 microdeletion syndrome
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
Autosomal dominant primary hypomagnesemia with hypocalciuria
Classic Mayer-Rokitansky-Küster-Hauser syndrome
Combined oxidative phosphorylation defect type 17
MURCS association
Renal cysts and diabetes syndrome
B-cell chronic lymphocytic leukemia
Hereditary nonpolyposis colon cancer
Precursor B-cell acute lymphoblastic leukemia
Seckel syndrome
Constitutional mismatch repair deficiency syndrome
Non-polyposis Turcot syndrome
Muir-Torre syndrome
Mantle cell lymphoma
Precursor T-cell acute lymphoblastic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Ataxia-telangiectasia variant
Combined cervical dystonia
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Amyotrophic lateral sclerosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Melanoma of soft part
Nijmegen breakage syndrome-like disorder
Adrenocortical carcinoma
Papilloma of choroid plexus
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Autosomal dominant nonsyndromic intellectual deficit
Chronic myeloid leukemia
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Familial melanoma
Split hand-split foot malformation
Williams syndrome
Familial congenital mirror movements
Severe combined immunodeficiency due to DNA-PKcs deficiency
Ataxia-telangiectasia-like disorder
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Adult-onset distal myopathy due to VCP mutation
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Jawad syndrome
Familial isolated dilated cardiomyopathy
Chronic intestinal pseudoobstruction
Chronic mucocutaneous candidiasis
Congenital short bowel syndrome
Congenital valvular dysplasia
Ehlers-Danlos syndrome with periventricular heterotopia
Frontometaphyseal dysplasia
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Susceptibility to viral and mycobacterial infections
Terminal osseous dysplasia - pigmentary defects
Coffin-Siris syndrome
Familial rhabdoid tumor
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute promyelocytic leukemia
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Leber congenital amaurosis
Partial androgen insensitivity syndrome
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Follicular lymphoma
Intravascular large B-cell lymphoma
Retinitis pigmentosa
Omenn syndrome
Severe combined immunodeficiency due to DCLRE1C deficiency
Xeroderma pigmentosum variant
Autosomal recessive primary microcephaly
Premature chromosome condensation with microcephaly and intellectual deficit
Inflammatory myofibroblastic tumor
Osteogenesis imperfecta type 3
Isolated scaphocephaly
COFS syndrome
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
UV-sensitive syndrome
Cornelia de Lange 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
Bloom syndrome
Burkitt lymphoma
Cowden syndrome
Estrogen resistance syndrome
Proteus syndrome
Anaplastic ependymoma
BAP1-related tumor predisposition syndrome
Multiple myeloma
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Budd-Chiari syndrome
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
X-linked distal arthrogryposis multiplex congenita
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Autosomal agammaglobulinemia
Mosaic variegated aneuploidy syndrome
SHORT syndrome
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
Spinocerebellar ataxia type 12
Angelman syndrome
Autosomal dominant spastic paraplegia type 13
Ewing sarcoma
Extraskeletal Ewing sarcoma
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Hyperinsulinism due to HNF1A deficiency
Isolated delta-storage pool disease
Left ventricular noncompaction
MODY syndrome
Paris-Trousseau thrombocytopenia
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Peripheral primitive neuroectodermal tumor
Weaver syndrome
Alpha-thalassemia - X-linked intellectual deficit syndrome
Alpha-thalassemia - myelodysplastic syndrome
Carpenter-Waziri syndrome
Chudley-Lowry-Hoar syndrome
Holmes-Gang syndrome
Intellectual deficit - sparse hair - brachydactyly
Juberg-Marsidi syndrome
Smith-Fineman-Myers syndrome
Werner syndrome
17q11 microdeletion syndrome
Autosomal recessive nonsyndromic intellectual deficit
Cone rod dystrophy
MMEP syndrome
Meckel syndrome
Senior-Loken syndrome
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
X-linked lymphoproliferative disease
Berardinelli-Seip congenital lipodystrophy
Chuvash erythrocytosis
Developmental delay with autism spectrum disorder and gait instability
Male infertility with normal virilization due to meiosis defect
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Von Hippel-Lindau disease
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
ADULT syndrome
ALK-positive anaplastic large cell lymphoma
ALK-positive large B-cell lymphoma
Alobar holoprosencephaly
Ankyloblepharon - ectodermal defects - cleft lip / palate
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant Larsen syndrome
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal dominant limb-girdle muscular dystrophy type 1F
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive limb-girdle muscular dystrophy type 2O
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal thrombocytopenia with normal platelets
Baraitser-Winter syndrome
Bladder exstrophy
Boomerang dysplasia
Branchio-oculo-facial syndrome
Caffey disease
Cap myopathy
Cerebellar ataxia - hypogonadism
Childhood-onset nemaline myopathy
Congenital dyserythropoietic anemia type III
Congenital fiber-type disproportion myopathy
Congenital muscular dystrophy with cerebellar involvement
Congenital stromal corneal dystrophy
Dehydratase deficiency
Dermatofibrosarcoma protuberans
Distal 16p11.2 microdeletion syndrome
Distal 22q11.2 microdeletion syndrome
Distal monosomy 3p
EEC syndrome
Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, vascular-like type
Ehlers-Danlos / osteogenesis imperfecta syndrome
Frontonasal dysplasia with alopecia and genital anomaly
Frontotemporal dementia with motor neuron disease
Gray platelet syndrome
Gräsbeck-Imerslund disease
High bone mass osteogenesis imperfecta
Hypocalcemic vitamin D-resistant rickets
Hypoparathyroidism - deafness - renal disease
Infantile Refsum disease
Intellectual deficit, X-linked, Nascimento type
Intellectual deficit, X-linked, Turner type
Intermediate nemaline myopathy
Leber hereditary optic neuropathy
Lethal acantholytic epidermolysis bullosa
Limb-mammary syndrome
Lobar holoprosencephaly
MELAS syndrome
Male infertility associated with large-headed multiflagellar polyploid spermatozoa
Maternally-inherited Leigh syndrome
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Muscle-eye-brain disease
Naxos disease
Neonatal adrenoleukodystrophy
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
Papillary or follicular thyroid carcinoma
Parietal foramina
Pontocerebellar hypoplasia type 1
Pontocerebellar hypoplasia type 2
Pontocerebellar hypoplasia type 4
Pontocerebellar hypoplasia type 5
Potocki-Shaffer syndrome
Primary biliary cirrhosis
Proximal 16p11.2 microdeletion syndrome
Renal coloboma syndrome
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
Smith-Magenis syndrome
Spondylocarpotarsal synostosis
Usher syndrome type 2
Usher syndrome type 3
Walker-Warburg syndrome
Zellweger syndrome
Autosomal dominant hyper-IgE syndrome
Familial capillary hemangioma
GAPO syndrome
Atypical teratoid tumor
Craniofrontonasal dysplasia
Crouzon disease
Familial lambdoid synostosis
Familial multiple meningioma
Isolated cloverleaf skull syndrome
Neurofibromatosis type 3
West syndrome
Aicardi-Goutières syndrome
Atypical juvenile parkinsonism
Cerebroretinal vasculopathy
Chilblain lupus
Familial isolated congenital asplenia
Generalized juvenile polyposis / juvenile polyposis coli
HERNS syndrome
Hereditary hemorrhagic telangiectasia
Hereditary vascular retinopathy
Metaphyseal anadysplasia
Myhre syndrome
Nodulosis-arthropathy-osteolysis syndrome
Torg-Winchester syndrome
X-linked non-syndromic intellectual deficit
Young adult-onset Parkinsonism
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
(no synonyms)

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

Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
External references:
19 OMIM references -
1 MeSH reference: C537243

No signs/symptoms info available.