Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Spinal Cord Diseases » Muscular Atrophy, Spinal » Bulbo-Spinal Atrophy, X-Linked
Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Heredodegenerative Disorders, Nervous System » Bulbo-Spinal Atrophy, X-Linked
Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Motor Neuron Disease » Muscular Atrophy, Spinal » Bulbo-Spinal Atrophy, X-Linked
Diseases [C] » Nervous System Diseases [C10] » Neuromuscular Diseases » Motor Neuron Disease » Muscular Atrophy, Spinal » Bulbo-Spinal Atrophy, X-Linked
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » Bulbo-Spinal Atrophy, X-Linked
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Heredodegenerative Disorders, Nervous System » Bulbo-Spinal Atrophy, X-Linked
Description
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR. MeSH
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Phase 4 Indicated Drugs (1)
Phase 2 Indicated Drugs (4)
Organization Involved with Phase 4 Indications (2)
Organization Involved with Phase 2 Indications (5)
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