Spinal Muscular Atrophies of Childhood

"Spinal Muscular Atrophies of Childhood" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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A group of recessively inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)

Descriptor ID	D014897
MeSH Number(s)	C10.228.854.468.800 C10.574.500.812 C10.574.562.500.750 C10.668.467.500.750 C16.320.400.765
Concept/Terms	Spinal Muscular Atrophies of Childhood Spinal Muscular Atrophies of Childhood Muscular Atrophy, Spinal, Type II Muscular Atrophy, Spinal, Type II Type II Spinal Muscular Atrophy Spinal Muscular Atrophy, Type II Spinal Muscular Atrophy Type 2 Spinal Muscular Atrophy Type II HMN (Hereditary Motor Neuropathy) Proximal Type I HMN (Hereditary Motor Neuropathy) Proximal Type I Muscular Atrophy, Infantile Atrophies, Infantile Muscular Atrophy, Infantile Muscular Infantile Muscular Atrophies Infantile Muscular Atrophy Muscular Atrophy, Spinal, Infantile Muscular Atrophy, Spinal, Type I Proximal Hereditary Motor Neuropathy Type I SMA, Infantile Acute Form Spinal Muscular Atrophy Type I Spinal Muscular Atrophy, Infantile Spinal Muscular Atrophy, Type I Type I Spinal Muscular Atrophy Werdnig Hoffman Disease Hoffman Disease, Werdnig Hoffman Diseases, Werdnig Werdnig Hoffman Diseases Werdnig-Hoffmann Disease Werdnig Hoffmann Disease Infantile Spinal Muscular Atrophy Spinal Muscular Atrophy 1 Juvenile Spinal Muscular Atrophy Juvenile Spinal Muscular Atrophy Kugelberg-Welander Syndrome Kugelberg Welander Syndrome Kugelberg-Welander Syndromes Muscular Atrophy, Juvenile Atrophies, Juvenile Muscular Atrophy, Juvenile Muscular Juvenile Muscular Atrophies Juvenile Muscular Atrophy Muscular Atrophies, Juvenile Muscular Atrophy, Spinal, Type III Type III Spinal Muscular Atrophy Spinal Muscular Atrophy, Juvenile Spinal Muscular Atrophy, Mild Childhood and Adolescent Form Spinal Muscular Atrophy, Type 3 Spinal Muscular Atrophy, Type III Kugelberg-Welander Disease Kugelberg Welander Disease Spinal Muscular Atrophy Type III

Below are MeSH descriptors whose meaning is more general than "Spinal Muscular Atrophies of Childhood".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Spinal Cord Diseases [C10.228.854]
Muscular Atrophy, Spinal [C10.228.854.468]
Spinal Muscular Atrophies of Childhood [C10.228.854.468.800]
Neurodegenerative Diseases [C10.574]
Heredodegenerative Disorders, Nervous System [C10.574.500]
Spinal Muscular Atrophies of Childhood [C10.574.500.812]
Motor Neuron Disease [C10.574.562]
Muscular Atrophy, Spinal [C10.574.562.500]
Spinal Muscular Atrophies of Childhood [C10.574.562.500.750]
Neuromuscular Diseases [C10.668]
Motor Neuron Disease [C10.668.467]
Muscular Atrophy, Spinal [C10.668.467.500]
Spinal Muscular Atrophies of Childhood [C10.668.467.500.750]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Spinal Muscular Atrophies of Childhood [C16.320.400.765]

Below are MeSH descriptors whose meaning is related to "Spinal Muscular Atrophies of Childhood".

Below are MeSH descriptors whose meaning is more specific than "Spinal Muscular Atrophies of Childhood".

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