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Familial atrial fibrillation
14 OMIM references -
17 associated genes
147 connected diseases
No signs/symptoms info
Disease Type of connection
Tetralogy of Fallot
Romano-Ward syndrome
Atrial septal defect, ostium secundum type
Single ventricular septal defect
Familial progressive cardiac conduction defect
Familial short QT syndrome
Jervell and Lange-Nielsen syndrome
Complete atrioventricular canal - ventricle hypoplasia
Familial isolated dilated cardiomyopathy
Brugada syndrome
46,XY partial gonadal dysgenesis
Athyreosis
Thyroid hypoplasia
Hypoplastic left heart syndrome
8p23.1 microdeletion syndrome
Atrial septal defect - atrioventricular conduction defects
Complete atrioventricular canal - Fallot tetralogy
Complete atrioventricular canal - left heart obstruction
Familial isolated congenital asplenia
Partial atrioventricular canal
Congenital diaphragmatic hernia
Axenfeld anomaly
Axenfeld-Rieger syndrome
Peters anomaly
Rieger anomaly
Acromegaloid facial appearance syndrome
Atrial stand still
Cardiodysrhythmic potassium-sensitive periodic paralysis
Dravet syndrome
Familial sick sinus syndrome
Generalized epilepsy with febrile seizures-plus context
Hypertrichotic osteochondrodysplasia, Cantu type
Idiopathic ventricular fibrillation, not Brugada type
Pancreatic hypoplasia - diabetes - congenital heart disease
Ring dermoid of cornea
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Catecholaminergic polymorphic ventricular tachycardia
Holt-Oram syndrome
Autosomal dominant hypohidrotic ectodermal dysplasia
Kabuki syndrome
MODY syndrome
Berardinelli-Seip congenital lipodystrophy
Lethal arthrogryposis - anterior horn cell disease
Lethal congenital contracture syndrome type 1
Acromesomelic dysplasia, Maroteaux type
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Tall stature - scoliosis - macrodactyly of the great toes
46,XX gonadal dysgenesis
46,XY complete gonadal dysgenesis
2q37 microdeletion syndrome
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
Reducing body myopathy
X-linked Emery-Dreifuss muscular dystrophy
X-linked myopathy with postural muscle atrophy
Athabaskan brainstem dysgenesis syndrome
Benign familial chorea
Benign familial infantile seizures
Benign familial neonatal seizures
Benign familial neonatal-infantile seizures
Bosley-Salih-Alorainy syndrome
Brain-lung-thyroid syndrome
Congenital analbuminemia
Congenital lethal myopathy, Compton-North type
Early infantile epileptic encephalopathy
Fibronectin glomerulopathy
Papillary or follicular thyroid carcinoma
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Oculodentodigital dysplasia
Syndactyly type 3
Distal 22q11.2 microdeletion syndrome
Hyperinsulinism due to HNF1A deficiency
17q11 microdeletion syndrome
1p36 deletion syndrome
Alveolar soft-part sarcoma
Aneurysm - osteoarthritis syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1C
Burkitt lymphoma
Chuvash erythrocytosis
Dedifferentiated liposarcoma
Diffuse cutaneous systemic sclerosis
Estrogen resistance syndrome
Familial melanoma
Familial pancreatic carcinoma
Familial thoracic aortic aneurysm and aortic dissection
Fanconi anemia
Frontonasal dysplasia with alopecia and genital anomaly
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Heritable pulmonary arterial hypertension
Hyperinsulinism due to HNF4A deficiency
Isolated scaphocephaly
Limited cutaneous systemic sclerosis
Myhre syndrome
Parietal foramina
Potocki-Shaffer syndrome
Precursor T-cell acute lymphoblastic leukemia
Pseudohypoaldosteronism type 2E
Rippling muscle disease
Translocation renal cell carcinoma
Von Hippel-Lindau disease
Weaver syndrome
Well-differentiated liposarcoma
17q23.1q23.2 microdeletion syndrome
Alobar holoprosencephaly
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
5q14.3 microdeletion syndrome
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Combined pituitary hormone deficiencies, genetic forms
Cystic fibrosis
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Panhypopituitarism
X-linked non-syndromic intellectual deficit
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 isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
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
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Progeria-associated arthropathy
Williams syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
14 OMIM references -
No MeSH references
No signs/symptoms info available.