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Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
11 associated genes
295 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial isolated dilated cardiomyopathy
Lethal acantholytic epidermolysis bullosa
Autosomal dominant Emery-Dreifuss muscular dystrophy
Keratosis palmoplantaris striata
Naxos disease
Idiopathic pulmonary fibrosis
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Catecholaminergic polymorphic ventricular tachycardia
Left ventricular noncompaction
Hutchinson-Gilford progeria syndrome
Lethal restrictive dermopathy
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Autosomal recessive centronuclear myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Early-onset myopathy with fatal cardiomyopathy
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
Hereditary proximal myopathy with early respiratory failure
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Mandibuloacral dysplasia with type A lipodystrophy
Progeria-associated arthropathy
Tibial muscular dystrophy
Amyotrophic lateral sclerosis
Autosomal dominant nonsyndromic intellectual deficit
Desmoid tumor
Familial thoracic aortic aneurysm and aortic dissection
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Hepatocellular carcinoma, childhood-onset
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Precursor T-cell acute lymphoblastic leukemia
Diffuse palmoplantar keratoderma with painful fissures
Focal palmoplantar keratoderma with joint keratoses
Severe dermatitis-multiple allergies-metabolic wasting syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Burkitt lymphoma
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Estrogen resistance syndrome
Hereditary nonpolyposis colon cancer
X-linked Emery-Dreifuss muscular dystrophy
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Localized epidermolysis bullosa simplex
Early-onset autosomal dominant Alzheimer disease
Pseudohypoaldosteronism type 2E
Hereditary breast and ovarian cancer syndrome
Loeys-Dietz syndrome type 1
46,XY partial gonadal dysgenesis
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Frontotemporal dementia with motor neuron disease
Familial gastric cancer
Gastric linitis plastica
Familial cerebral saccular aneurysm
Childhood-onset nemaline myopathy
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Congenital analbuminemia
Pulverulent cataract
Hereditary hemorrhagic telangiectasia
Giant cell glioblastoma
Adult-onset distal myopathy due to VCP mutation
Autosomal dominant centronuclear myopathy
Benign Samaritan congenital myopathy
Central core disease
Chronic intestinal pseudoobstruction
Congenital multicore myopathy with external ophthalmoplegia
Congenital short bowel syndrome
Congenital valvular dysplasia
Dowling-Degos disease
Ehlers-Danlos syndrome with periventricular heterotopia
Epidermolysis bullosa simplex with circinate migratory erythema
Frontometaphyseal dysplasia
King-Denborough syndrome
Malignant hyperthermia
Moderate multiminicore disease with hand involvement
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia type 12
Terminal osseous dysplasia - pigmentary defects
Heritable pulmonary arterial hypertension
Autosomal dominant limb-girdle muscular dystrophy type 1E
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency
Scapuloperoneal amyotrophy
Autosomal recessive limb-girdle muscular dystrophy type 2T
Cabezas syndrome
Congenital muscular dystrophy with cerebellar involvement
Congenital muscular dystrophy with intellectual disability
Fibronectin glomerulopathy
Glycogen storage disease due to muscle beta-enolase deficiency
Glycogen storage disease due to muscle glycogen phosphorylase deficiency
Isolated growth hormone deficiency type IA
Isolated growth hormone deficiency type IB
Isolated growth hormone deficiency type II
Muscle-eye-brain disease
Short stature due to growth hormone qualitative anomaly
Wolf-Hirschhorn syndrome
Young adult-onset Parkinsonism
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Hypoplastic left heart syndrome
Oculodentodigital dysplasia
Syndactyly type 3
Berardinelli-Seip congenital lipodystrophy
Generalized junctional epidermolysis bullosa, non-Herlitz type
Localized junctional epidermolysis bullosa, non-Herlitz type
Constitutional mismatch repair deficiency syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Non-polyposis Turcot syndrome
Papillary or follicular thyroid carcinoma
Reducing body myopathy
X-linked myopathy with postural muscle atrophy
Acute promyelocytic leukemia
Epidermolysis bullosa simplex with pyloric atresia
APC-related attenuated familial adenomatous polyposis
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Turcot syndrome with polyposis
Autosomal dominant macrothrombocytopenia
Autosomal recessive limb-girdle muscular dystrophy type 2G
Marfan syndrome type 2
Multiple keratoacanthoma, Ferguson-Smith type
Autosomal recessive ataxia, Beauce type
Autosomal recessive myogenic arthrogryposis multiplex congenita
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Autosomal recessive limb girdle muscular dystrophy type 2A
Adult-onset autosomal dominant leukodystrophy
Split hand-split foot malformation
Familial pancreatic carcinoma
3M syndrome
Epidermolysis bullosa simplex due to plakophilin deficiency
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
8p11.2 deletion syndrome
Annular epidermolytic ichthyosis
Epidermolytic ichthyosis
Epidermolytic palmoplantar keratoderma
Hereditary spherocytosis
Ichthyosis hystrix of Curth-Macklin
Brugada syndrome
Digitotalar dysmorphism
Early-onset generalized limb-onset dystonia
Exfoliative ichthyosis
Familial prostate cancer
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Lethal congenital contracture syndrome type 3
Myoclonus-dystonia syndrome
Timothy syndrome
EEM syndrome
Hypotrichosis with juvenile macular degeneration
Hereditary hypotrichosis with recurrent skin vesicles
Common variable immunodeficiency
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1
Leber congenital amaurosis
Nuclear cataract
Senior-Loken syndrome
X-linked Charcot-Marie-Tooth disease type 1
X-linked progressive cerebellar ataxia
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Primary peritoneal carcinoma
Adult hepatocellular carcinoma
Congenital non-bullous ichthyosiform erythroderma
Familial primary hypomagnesemia with normocalcuria and normocalcemia
Lamellar ichthyosis
Self-healing collodion baby
Fatal infantile hypertonic myofibrillar myopathy
Late-onset junctional epidermolysis bullosa
Posterior polar cataract
Zonular cataract
3-phosphoglycerate dehydrogenase deficiency
3C syndrome
Aicardi-Goutières syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1D
Autosomal dominant optic atrophy plus syndrome
Autosomal dominant optic atrophy, classic type
Autosomal dominant spastic paraplegia type 8
Autosomal recessive epidermolysis bullosa simplex
Autosomal recessive limb-girdle muscular dystrophy type 2B
Autosomal recessive limb-girdle muscular dystrophy type 2C
B-cell chronic lymphocytic leukemia
Bruck syndrome
Chilblain lupus
Combined immunodeficiency due to STK4 deficiency
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Congenital myopathy, Paradas type
Dermatopathia pigmentosa reticularis
Distal myopathy with anterior tibial onset
Familial hemophagocytic lymphohistiocytosis
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial isolated restrictive cardiomyopathy
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Miyoshi myopathy
Mosaic variegated aneuploidy syndrome
Muir-Torre syndrome
Naegeli-Franceschetti-Jadassohn syndrome
Nestor-Guillermo progeria syndrome
Pontocerebellar hypoplasia type 1
Pyogenic arthritis - pyoderma gangrenosum - acne
Romano-Ward syndrome
Severe combined immunodeficiency due to DNA-PKcs deficiency
Squamous cell carcinoma of head and neck
Fanconi anemia
Aneurysm - osteoarthritis syndrome
Translocation renal cell carcinoma
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Fuchs endothelial corneal dystrophy
Moyamoya disease
Pachyonychia congenita
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Autoimmune lymphoproliferative syndrome
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Diffuse cutaneous systemic sclerosis
Limited cutaneous systemic sclerosis
Peters anomaly
Spinocerebellar ataxia type 15 / 16
Spinocerebellar ataxia type 29
12q14 microdeletion syndrome
Acute necrotizing encephalopathy of childhood
Ataxia-telangiectasia-like disorder
Autosomal recessive limb-girdle muscular dystrophy type 2Q
Autosomal recessive nonsyndromic intellectual deficit
Autosomal thrombocytopenia with normal platelets
Buschke-Ollendorff syndrome
Distal 22q11.2 microdeletion syndrome
Dubin-Johnson syndrome
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex, Ogna type
Extraskeletal Ewing sarcoma
Familial acute necrotizing encephalopathy
Familial atrial fibrillation
Greenberg dysplasia
Hypotrichosis simplex
Inflammatory myofibroblastic tumor
Isolated osteopoikilosis
Junctional epidermolysis bullosa - pyloric atresia
Juvenile amyotrophic lateral sclerosis
Mandibuloacral dysplasia with type B lipodystrophy
Melorheostosis with osteopoikilosis
Methylmalonic acidemia with homocystinuria, type cblX
Myxoid / round cell liposarcoma
Partial acquired lipodystrophy
Renal tubular dysgenesis of genetic origin
Reticular dysgenesis
Reynolds syndrome
Sjögren-Larsson syndrome
TARP syndrome
Williams syndrome
Wolfram syndrome
X-linked non-syndromic intellectual deficit
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
- Familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the circulatory system -

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

No signs/symptoms info available.