Autism diagnosis codes
- Coding system
- SNOMED CT
- Coding system release
- unknown
- Organisation
- NHSD Primary Care Domain Refsets
- Codelist ID
- nhsd-primary-care-domain-refsets/autism_cod
- Version Tag
- 20200812
- Version ID
- 5b39356f
Versions
- 20210127
- 20200812
Description
Taken from the AUTISM_COD refset published by NHSD.
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 191689008 | Active infantile autism |
| 191690004 | Residual infantile autism |
| 191692007 | Active disintegrative psychoses |
| 191693002 | Residual disintegrative psychoses |
| 231536004 | Atypical autism |
| 23560001 | Asperger's disorder |
| 35919005 | Pervasive developmental disorder |
| 373618009 | Autistic spectrum disorder with isolated skills |
| 39951000119105 | Pervasive developmental disorder of residual state |
| 408856003 | Autistic disorder |
| 408857007 | Infantile autism |
| 432091002 | Savant syndrome |
| 43614003 | Autistic disorder of childhood onset |
| 442314000 | Active but odd autism |
| 68618008 | Rett's disorder |
| 702356009 | X-linked intellectual disability-psychosis-macroorchidism syndrome |
| 702450004 | FOXG1 syndrome |
| 702732007 | High-functioning autism |
| 708037001 | Residual Asperger's disorder |
| 712884004 | Pathological demand avoidance |
| 718393002 | Atypical Rett syndrome |
| 719600006 | 1p21.3 microdeletion syndrome |
| 71961003 | Childhood disintegrative disorder |
| 722287002 | Autism and facial port-wine stain syndrome |
| 723332005 | Isodicentric chromosome 15 syndrome |
| 733623005 | Autism spectrum disorder, epilepsy, arthrogryposis syndrome |
| 766824003 | Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder |
| 770790004 | Developmental delay with autism spectrum disorder and gait instability |
| 771448004 | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency |
| 771512003 | Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency |
| 783089006 | Macrocephaly, intellectual disability, autism syndrome |
Codes not in the full codelist are in faint grey.