Departments of Anesthesiology and Biostatistics | University of Michigan

ICD mappings

ICD code Type Description Phenome
G12.0 ICD10CM Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] MGI
G12.1 ICD10CM Other inherited spinal muscular atrophy MGI
G12.2 ICD10CM Motor neuron disease MGI
G12.20 ICD10CM Motor neuron disease, unspecified MGI
G12.21 ICD10CM Amyotrophic lateral sclerosis MGI
G12.22 ICD10CM Progressive bulbar palsy MGI
G12.23 ICD10CM Primary lateral sclerosis MGI
G12.24 ICD10CM Familial motor neuron disease MGI
G12.25 ICD10CM Progressive spinal muscle atrophy MGI
G12.29 ICD10CM Other motor neuron disease MGI
G12.8 ICD10CM Other spinal muscular atrophies and related syndromes MGI
G12.9 ICD10CM Spinal muscular atrophy, unspecified MGI
335.0 ICD9CM Werdnig-Hoffmann disease MGI
335.10 ICD9CM Spinal muscular atrophy, unspecified MGI
335.11 ICD9CM Kugelberg-Welander disease MGI
335.19 ICD9CM Other spinal muscular atrophy MGI
335.20 ICD9CM Amyotrophic lateral sclerosis MGI
335.21 ICD9CM Progressive muscular atrophy MGI
335.22 ICD9CM Progressive bulbar palsy MGI
335.23 ICD9CM Pseudobulbar palsy MGI
335.24 ICD9CM Primary lateral sclerosis MGI
335.29 ICD9CM Other motor neuron disease MGI
335.8 ICD9CM Other anterior horn cell diseases MGI
335.9 ICD9CM Anterior horn cell disease, unspecified MGI
G12.0 ICD10 G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] UKB
G12.1 ICD10 G12.1 Other inherited spinal muscular atrophy UKB
G12.2 ICD10 G12.2 Motor neuron disease UKB
G12.8 ICD10 G12.8 Other spinal muscular atrophies and related syndromes UKB
G12.9 ICD10 G12.9 Spinal muscular atrophy, unspecified UKB
335 ICD9 335 Anterior horn cell disease UKB
335.0 ICD9 3350 Werdnig-hoffman disease UKB
335.1 ICD9 3351 Spinal muscular atrophy UKB
335.2 ICD9 3352 Motor neurone disease UKB
335.8 ICD9 3358 Other specified anterior horn cell disease UKB
335.9 ICD9 3359 Anterior horn cell disease, unspecified UKB

This page is mainly a phenotype dictionary entry. When you are trying to find candidate PRS models, go to the Scores table, search by trait or exposure name, and then use the score-detail and PheWAS pages for model-specific follow-up.

Found a bug?

Report a PRSweb issue

Open an email draft

This uses your default mail app and includes the current page URL automatically.