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Neuralgic amyotrophy
1 OMIM reference -
1 associated gene
45 connected diseases
15 signs/symptoms
Disease Type of connection
Giant cell glioblastoma
Gliosarcoma
Fibronectin glomerulopathy
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Autosomal dominant hypohidrotic ectodermal dysplasia
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
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
Adult-onset proximal spinal muscular atrophy, autosomal dominant
Amyotrophic lateral sclerosis
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Autosomal dominant spastic paraplegia type 13
Boomerang dysplasia
Cap myopathy
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Constitutional mismatch repair deficiency syndrome
Fatal infantile cytochrome C oxidase deficiency
Fatal infantile lactic acidosis with methylmalonic aciduria
Hereditary nonpolyposis colon cancer
Inflammatory myofibroblastic tumor
Intermediate nemaline myopathy
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with cardiomyopathy
Leukoencephalopathy - dystonia - motor neuropathy
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Rare isolated myopia
Spondylocarpotarsal synostosis
X-linked myopathy with excessive autophagy
Synonym(s):
- Acute brachial plexus neuritis
- Brachial plexus neuritis
- Immune brachial plexus neuropathy
- Mononeuritis multiplex with brachial predilection
- Neuralgic shoulder amyotrophy
- Serum neuritis
- Winged scapula
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 6-9 / 10 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SEPT9 Q9UHD8604061
Very frequent
- Abnormal EMG / electromyogram / electropmyography
- Articular / joint pain / arthralgia
- Muscle weakness / flaccidity
- Neuritis / polyneuritis / multineuritis

Frequent
- Paresthesia / dysesthesia / hypoesthesia / anesthesia / numbness
- Scapula structural / position anomaly / congenital elevation / Sprengel anomaly

Occasional
- Acrocyanosis / Raynaud's phenomenon / vasomotor disorders
- Cleft lip and palate
- Elocution disorders / dysarthria / dysphonia
- Microstomia / little mouth
- Peripheral neuropathy
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Round face
- Short stature / dwarfism / nanism
- Sleep and vigilance disorders