intermediate spinal muscular atrophy
Human disease
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intermediate spinal muscular atrophy
Summary
intermediate spinal muscular atrophy is a rare disease[1].
Key Facts
- intermediate spinal muscular atrophy's instance of is recorded as rare disease[2].
- intermediate spinal muscular atrophy's instance of is recorded as class of disease[3].
- intermediate spinal muscular atrophy is a type of survival motor neuron spinal muscular atrophy[4].
- intermediate spinal muscular atrophy is a type of genetic disease[5].
- intermediate spinal muscular atrophy is a type of autosomal recessive disease[6].
- intermediate spinal muscular atrophy's ICD-9-CM is recorded as 335.19[7].
- intermediate spinal muscular atrophy's NCI Thesaurus ID is recorded as C156310[8].
- intermediate spinal muscular atrophy's genetic association is recorded as SMN1[9].
- intermediate spinal muscular atrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050530[10].
- intermediate spinal muscular atrophy's exact match is recorded as http://identifiers.org/doid/DOID:0050530[11].
- intermediate spinal muscular atrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_70[12].
- intermediate spinal muscular atrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_83418[13].
- intermediate spinal muscular atrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].