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Term:
atrophic muscular disease
(DOID:913)
Annotations:
Rat: (427)
Mouse: (419)
Human: (483)
Chinchilla: (396)
Bonobo: (415)
Dog: (418)
Squirrel: (404)
Pig: (416)
Parent Terms
Term With Siblings
Child Terms
muscle tissue disease
+
muscular disease
+
3-Methylcrotonyl-CoA carboxylase deficiency
+
arthrogryposis multiplex congenita
+
atrophic muscular disease
+
A neuromuscular disease that is characterized by an abnormal reduction in the muscle volume and atrophy. (DO)
Axial Myopathy, Late-Onset
+
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia
Carey-Fineman-Ziter syndrome
+
chronic fatigue syndrome
compartment syndrome
+
Congenital Myopathy with Neuropathy and Deafness
Congenital Universal Muscular Hypoplasia of Krabbe
Contracture
+
Craniomandibular Disorders
+
cysticercosis
+
diaphragm disease
+
Dimauro Disease
distal arthrogryposis
+
Early-Onset Myopathy with Fatal Cardiomyopathy
Ehlers-Danlos syndrome kyphoscoliotic type 2
eosinophilia-myalgia syndrome
epidemic pleurodynia
Erythrocyte Amp Deaminase Deficiency
Erythrocyte Lactate Transporter Defect
familial periodic paralysis
+
fibromyalgia
+
Fingerprint Body Myopathy
Gamstorp-Wohlfart syndrome
gas gangrene
Granulovacuolar Lobular Myopathy with Electrical Myotonia
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis
Hypertrophia Musculorum Vera
Internal Anal Sphincter Myopathy
Kocher-Debre-Semelaigne Syndrome
Late-Onset Carnitine Palmitoyltransferase II Deficiency
malignant hyperthermia
+
Marinesco-Sjogren syndrome
Medial Tibial Stress Syndrome
Mitochondrial DNA Depletion Syndrome, Myopathic Form
+
Muscle Cramp
+
Muscle Rigidity
+
Muscle Spasticity
+
muscle tissue disease
+
Muscle Tissue Neoplasms
+
Muscle Weakness
+
Musculoskeletal Pain
+
Myalgia
+
myofascial pain syndrome
+
Myopathic Carnitine Deficiency
myopathy
+
Myopathy with Lactic Acidosis, Hereditary
myostatin-related muscle hypertrophy
myotonic disease
+
Myotoxicity
neutral lipid storage disease
+
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Pectoralis Muscle, Absence of
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss
Proximal Myopathy with Focal Depletion of Mitochondria
Rhabdomyolysis
+
rippling muscle disease 1
Singleton Merten Syndrome
+
sinoatrial node disease
+
Skeletal Muscle Injuries
Skeletal Muscle Reperfusion Injury
systemic primary carnitine deficiency disease
Tel Hashomer Camptodactyly Syndrome
tendinitis
+
toxocariasis
+
Treft Sanborn Carey Syndrome
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy
Uruguay faciocardiomusculoskeletal syndrome
Vacuolar Myopathy
very long chain acyl-CoA dehydrogenase deficiency
Brody myopathy
Charcot-Marie-Tooth disease X-linked recessive 5
Congenital Myopathy with Fast-Twitch (Type ii) Fiber Atrophy
muscular dystrophy
+
postpoliomyelitis syndrome
Synonyms
Exact Synonyms:
Disuse Atrophy ; Spinobulbar Atrophies ; atrophic muscular disorder ; atrophic muscular disorders ; disuse atrophies ; spinobulbar atrophy ; spinopontine atrophies ; spinopontine atrophy
Narrow Synonyms:
distal lower limb amyotrophy
Primary IDs:
MESH:D020966
Xrefs:
EFO:0009912
;
NCI:C84574
Definition Sources:
https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&version=14.10d&code=C84574
"DO" "DO"