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Muscular dystrophy, Selcen type
1 OMIM reference -
1 associated gene
152 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
Amyotrophic lateral sclerosis
Distal hereditary motor neuropathy type 2
Autosomal dominant Charcot-Marie-Tooth disease type 2L
Cerebellar ataxia - hypogonadism
Follicular lymphoma
Intravascular large B-cell lymphoma
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Autosomal dominant limb-girdle muscular dystrophy type 1D
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
17p13.3 microduplication syndrome
46,XY disorder of sex development due to isolated 17, 20 lyase deficiency
Acute necrotizing encephalopathy of childhood
Aneurysm - osteoarthritis syndrome
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Anophthalmia / microphthalmia - esophageal atresia
Argininosuccinic aciduria
Arnold-Chiari malformation type II
Atypical Gaucher disease due to saposin C deficiency
Auriculocondylar syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2B
Autosomal recessive cutis laxa type 2B
Autosomal recessive limb-girdle muscular dystrophy type 2Q
B-cell chronic lymphocytic leukemia
Birt-Hogg-Dube syndrome
Branchio-oculo-facial syndrome
Cabezas syndrome
Caudal regression sequence
Cervical spina bifida aperta
Cervical spina bifida cystica
Cervicothoracic spina bifida aperta
Cervicothoracic spina bifida cystica
Charcot-Marie-Tooth disease type 1C
Childhood absence epilepsy
Coats disease
Colobomatous microphthalmia
Common variable immunodeficiency
Congenital amegakaryocytic thrombocytopenia
Congenital non-communicating hydrocephalus
Dent disease type 1
Distal 17p13.3 microdeletion syndrome
Distal 22q11.2 microdeletion syndrome
Distal monosomy 3p
Dyskeratosis congenita
Early infantile epileptic encephalopathy
Encephalopathy due to prosaposin deficiency
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex with pyloric atresia
Epidermolysis bullosa simplex, Ogna type
Erythrocyte galactose epimerase deficiency
Essential thrombocythemia
Familial acute necrotizing encephalopathy
Familial exudative vitreoretinopathy
Familial isolated congenital asplenia
Familial spontaneous pneumothorax
Familial thoracic aortic aneurysm and aortic dissection
Familial thrombocytosis
Fetal akinesia deformation sequence
Fragile X syndrome
Fragile X-associated tremor / ataxia syndrome
Galactokinase deficiency
Gamma-aminobutyric acid transaminase deficiency
Generalized congenital lipodystrophy with myopathy
Generalized galactose epimerase deficiency
Geroderma osteodysplastica
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
Hemolytic anemia due to glucophosphate isomerase deficiency
Hepatoerythropoietic porphyria
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
Hereditary sensory and autonomic neuropathy type 2
Hoyeraal-Hreidarsson syndrome
Hutchinson-Gilford progeria syndrome
Hyper-IgM syndrome type 3
Hyperphosphatasia-intellectual deficiency syndrome
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Infantile Krabbe disease
Inflammatory myofibroblastic tumor
Isolated anophthalmia - microphthalmia
Isolated growth hormone deficiency type IA
Isolated growth hormone deficiency type IB
Isolated growth hormone deficiency type II
Juvenile myoclonic epilepsy
Juvenile rheumatoid factor-negative polyarthritis
Late-onset autosomal recessive medullary cystic kidney disease
Left ventricular noncompaction
Lethal multiple pterygium syndrome
Lethal restrictive dermopathy
Lumbosacral spina bifida aperta
Lumbosacral spina bifida cystica
Machado-Joseph disease type 1
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Mandibuloacral dysplasia with type B lipodystrophy
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Miller-Dieker syndrome
Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
Myelofibrosis with myeloid metaplasia
Nager syndrome
Norrie disease
Oligoarticular juvenile arthritis
PYCR1-related DeBarsy syndrome
Pediatric systemic lupus erythematosus
Persistent hyperplastic primary vitreous
Phosphoserine aminotransferase deficiency
Polycythemia vera
Porphyria cutanea tarda
Postsynaptic congenital myasthenic syndromes
Primary ciliary dyskinesia
Pseudohypoaldosteronism type 2C
Pulverulent cataract
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Reticular dysgenesis
Retinopathy - anemia- central nervous system anomalies
Retinopathy of prematurity
Septo-optic dysplasia
Severe X-linked mitochondrial encephalomyopathy
Severe combined immunodeficiency due to DNA-PKcs deficiency
Short stature due to growth hormone qualitative anomaly
Simpson-Golabi-Behmel syndrome
Split hand-split foot malformation
Thoracolumbosacral spina bifida aperta
Thoracolumbosacral spina bifida cystica
Total spina bifida aperta
Total spina bifida cystica
Unverricht-Lundborg disease
Upper thoracic spina bifida aperta
Upper thoracic spina bifida cystica
Wiskott-Aldrich syndrome
X-linked Charcot-Marie-Tooth disease type 4
X-linked distal arthrogryposis multiplex congenita
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
X-linked non-syndromic intellectual deficit
Xq27.3q28 duplication syndrome
Young adult-onset Parkinsonism
ZASP-related myofibrillar myopathy
Acute promyelocytic leukemia
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Distal hereditary motor neuropathy type 7
Perry syndrome
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
BAG3 O95817603883
No signs/symptoms info available.