Spinal muscular atrophy with lower extremity predominance 772129007

SNOMED CT code

SNOMED code

772129007

name

Spinal muscular atrophy with lower extremity predominance

status

active

date introduced

2019-01-31

fully specified name(s)

Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder)

synonyms

Autosomal dominant childhood-onset proximal spinal muscular atrophy
Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy
SMALED - spinal muscular atrophy, lower extremity, dominant
Spinal muscular atrophy with lower extremity predominance

attributes - group1

Finding site

Nervous system structure 25087005

parents

Autosomal dominant hereditary disorder 11164009
Spinal muscular atrophy 5262007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Spinal muscular atrophy with lower extremity predominance 772129007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of nervous system 118940003
Hereditary disorder of nervous system 363235000
Hereditary motor neuron disease 49793008
Spinal muscular atrophy 5262007
Spinal muscular atrophy with lower extremity predominance 772129007

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Spinal muscular atrophy 5262007
Autosomal hereditary disorder 1899006
Hereditary motor neuron disease 49793008
Lower motor neuron disease 84590007
Hereditary disorder of nervous system 363235000
Motor neuron disease 37340000
Disorder of nervous system 118940003
Hereditary disorder by system 363137000
Hereditary disease 32895009
Disorder of body system 362965005
Genetic disease 782964007
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Spinal muscular atrophy with lower extremity predominance 772129007

SNOMED CT code