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Romano-Ward syndrome
11 OMIM references -
13 associated genes
130 connected diseases
No signs/symptoms info
Disease Type of connection
Familial atrial fibrillation
Familial short QT syndrome
Jervell and Lange-Nielsen syndrome
Familial isolated dilated cardiomyopathy
Atrial stand still
Brugada syndrome
Familial progressive cardiac conduction defect
Familial sick sinus syndrome
Idiopathic ventricular fibrillation, not Brugada type
Autosomal dominant limb-girdle muscular dystrophy type 1C
Rippling muscle disease
Familial hyperaldosteronism type 3
Catecholaminergic polymorphic ventricular tachycardia
Giant cell glioblastoma
Gliosarcoma
Becker muscular dystrophy
Duchenne muscular dystrophy
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
Idiopathic hypereosinophilic syndrome
Dravet syndrome
Generalized epilepsy with febrile seizures-plus context
Precursor B-cell acute lymphoblastic leukemia
Benign familial infantile seizures
Benign familial neonatal-infantile seizures
Early infantile epileptic encephalopathy
Essential thrombocythemia
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Leprechaunism
Rabson-Mendenhall syndrome
X-linked non-syndromic intellectual deficit
Left ventricular noncompaction
Autosomal recessive limb-girdle muscular dystrophy type 2P
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
X-linked epilepsy - learning disabilities - behavior disorders
Apolipoprotein A-I deficiency
Tangier disease
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Autosomal dominant hypohidrotic ectodermal dysplasia
Donnai-Barrow syndrome
Autosomal dominant nonsyndromic intellectual deficit
Familial advanced sleep-phase syndrome
Epilepsy with myoclonic-astatic seizures
Familial or sporadic hemiplegic migraine
Lennox-Gastaut syndrome
Malignant migrating partial seizures of infancy
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Gastrointestinal stromal tumor
Hereditary spherocytosis
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRA rearrangement
Myeloid neoplasm associated with PDGFRB rearrangement
Oligodontia
Unclassified chronic myeloproliferative disease
Autosomal recessive limb-girdle muscular dystrophy type 2B
Congenital myopathy, Paradas type
Distal myopathy with anterior tibial onset
Glycogen storage disease due to muscle phosphofructokinase deficiency
Miyoshi myopathy
Benign familial neonatal seizures
Congenital analbuminemia
Hereditary nonpolyposis colon cancer
17q11 microdeletion syndrome
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Autosomal recessive primary microcephaly
Cerebellar ataxia - hypogonadism
Childhood-onset nemaline myopathy
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Generalized epilepsy - paroxysmal dyskinesia
Hereditary hypophosphatemic rickets with hypercalciuria
Hyperparathyroidism - jaw tumor syndrome
Inherited acute myeloid leukemia
Intermediate nemaline myopathy
Isolated NADH-CoQ reductase deficiency
Juvenile amyotrophic lateral sclerosis
Megalencephalic leukoencephalopathy with subcortical cysts
Myelofibrosis with myeloid metaplasia
Parathyroid carcinoma
Pyogenic arthritis - pyoderma gangrenosum - acne
Severe congenital nemaline myopathy
T-cell immunodeficiency with epidermodysplasia verruciformis
Typical nemaline myopathy
Acetazolamide-responsive myotonia
Hyperkalemic periodic paralysis
Hypokalemic periodic paralysis
Microcephalic osteodysplastic primordial dwarfism type 2
Myotonia fluctuans
Myotonia permanens
Paramyotonia congenita of Von Eulenburg
Postsynaptic congenital myasthenic syndromes
Seckel syndrome
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Cystic fibrosis
Early-onset autosomal dominant Alzheimer disease
Familial pancreatic carcinoma
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
Li-Fraumeni syndrome
Papilloma of choroid plexus
West syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Familial thoracic aortic aneurysm and aortic dissection
Hirschsprung disease
Hydrocephalus with stenosis of aqueduct of Sylvius
Juvenile myelomonocytic leukemia
MASA syndrome
Moyamoya disease
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
X-linked complicated corpus callosum dysgenesis
X-linked complicated spastic paraplegia type 1
Charcot-Marie-Tooth disease type 4B1
Immunodeficiency due to CD25 deficiency
Infantile dystonia-parkinsonism
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Precursor T-cell acute lymphoblastic leukemia
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
Synonym(s):
- Romano-Ward long QT syndrome
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
11 OMIM references -
1 MeSH reference: D029597
No signs/symptoms info available.