Preferred Name |
Spinal_Muscular_Atrophy |
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Synonyms |
|
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ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Spinal_Muscular_Atrophy |
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ID |
C85075 |
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NCI_Definition |
An inherited disorder characterized by degeneration of the spinal cord and the cerebellum. Symptoms may appear at any age and include progressive loss of coordination of gait, hands, speech, and eye movements. |
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NCI_PT |
Spinal Muscular Atrophy |
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NICHD_Definition |
_ |
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prefixIRI |
Spinal_Muscular_Atrophy |
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prefLabel |
Spinal_Muscular_Atrophy |
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Subset_Association1 |
NICHD Pediatric Terminology |
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Subset_Association2 |
Neonatal Research Network Terminology |
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SYN | ||
subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Abnormality_of_the_Nervous_System |
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