MedlinePlus Health Topics

Last uploaded: January 29, 2019
Preferred Name

SMA

Synonyms

Spinal Muscular Atrophy

Definitions

<p>Spinal muscular atrophy (SMA) is a genetic disease that attacks nerve cells, called motor neurons, in the spinal cord. These cells communicate with your voluntary muscles - the ones you can control, like in your arms and legs. As the neurons die, the muscles weaken. This can affect walking, crawling, breathing, swallowing, and head and neck control.</p> <p>SMA runs in families. Parents usually have no symptoms, but still carry the gene. Genetic counseling is important if the disease runs in your family.</p> <p>There are many types of SMA. Some of them are fatal. Some people have a normal life expectancy. It depends on the type and how it affects breathing. There is no cure. Treatments help with symptoms and prevent complications. They may include machines to help with breathing, nutritional support, physical therapy, and medicines.</p> <p >NIH: National Institute of Neurological Disorders and Stroke</p>

ID

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026847

altLabel

Spinal Muscular Atrophy

cui

C0026847

Date created

06/27/2002

definition

Spinal muscular atrophy (SMA) is a genetic disease that attacks nerve cells, called motor neurons, in the spinal cord. These cells communicate with your voluntary muscles - the ones you can control, like in your arms and legs. As the neurons die, the muscles weaken. This can affect walking, crawling, breathing, swallowing, and head and neck control.

SMA runs in families. Parents usually have no symptoms, but still carry the gene. Genetic counseling is important if the disease runs in your family.

There are many types of SMA. Some of them are fatal. Some people have a normal life expectancy. It depends on the type and how it affects breathing. There is no cure. Treatments help with symptoms and prevent complications. They may include machines to help with breathing, nutritional support, physical therapy, and medicines.

NIH: National Institute of Neurological Disorders and Stroke

Inverse of RQ

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Inverse of SY

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026847

Mapped from

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026847

Mapped to

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026847

MP HEALTH TOPIC URL

https://medlineplus.gov/spinalmuscularatrophy.html

MP OTHER LANGUAGE URL

Spanish https://medlineplus.gov/spanish/spinalmuscularatrophy.html

MP PRIMARY INSTITUTE URL

National Institute of Neurological Disorders and Stroke http://www.ninds.nih.gov/

notation

C0026847

prefLabel

SMA

Related to

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027868

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0037928

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026850

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MEDLINEPLUS/C1456603

http://purl.bioontology.org/ontology/MEDLINEPLUS/C2362500

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/D009134 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/OMIM/MTHU047788 Online Mendelian Inheritance in Man CUI
http://purl.bmicc.cn/ontology/ICD10CN/G12.9 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10CM/G12.9 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10/G12.9 International Classification of Diseases, Version 10 CUI