infantile-onset X-linked spinal muscular atrophy

Summary

infantile-onset X-linked spinal muscular atrophy is a class of disease^[1].

Key Facts

• infantile-onset X-linked spinal muscular atrophy's instance of is recorded as class of disease^[2].
• infantile-onset X-linked spinal muscular atrophy's subclass of is recorded as nervous system heredodegenerative disease^[3].
• infantile-onset X-linked spinal muscular atrophy's MeSH descriptor ID is recorded as C535380^[4].
• infantile-onset X-linked spinal muscular atrophy's OMIM ID is recorded as 301830^[5].
• infantile-onset X-linked spinal muscular atrophy's Orphanet ID is recorded as 1145^[6].
• infantile-onset X-linked spinal muscular atrophy's genetic association is recorded as UBA1^[7].
• infantile-onset X-linked spinal muscular atrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1145^[8].
• infantile-onset X-linked spinal muscular atrophy's UMLS CUI is recorded as C1844934^[9].
• infantile-onset X-linked spinal muscular atrophy's ICD-10-CM is recorded as G12.1^[10].
• infantile-onset X-linked spinal muscular atrophy's Mondo ID is recorded as MONDO_0010532^[11].