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Duchenne muscular dystrophy
1 OMIM reference -
2 associated genes
38 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
Becker muscular dystrophy
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
Left ventricular noncompaction
Romano-Ward syndrome
Autosomal recessive limb-girdle muscular dystrophy type 2P
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Spinocerebellar ataxia type 7
Congenital analbuminemia
Alternating hemiplegia of childhood
Benign paroxysmal torticollis of infancy
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Spinocerebellar ataxia type 6
B-cell chronic lymphocytic leukemia
Dentatorubral pallidoluysian atrophy
Distal 22q11.2 microdeletion syndrome
Generalized congenital lipodystrophy with myopathy
Gray platelet syndrome
Synpolydactyly type 2
Atrial septal defect, ostium secundum type
Camurati-Engelmann disease
Cystic fibrosis
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
Autoimmune lymphoproliferative syndrome
Synonym(s):
- DMD
- Severe dystrophinopathy, Duchenne type
Classification (Orphanet):
- Rare cardiac disease
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: young adult
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
1 MeSH reference: D020388
Gene symbol UniProt reference OMIM reference
DMD P11532300377
LTBP4 Q8N2S1604710
No signs/symptoms info available.