Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008

SNOMED CT code

SNOMED code

763798008

name

Microcephalus, complex motor and sensory axonal neuropathy syndrome

status

active

date introduced

2018-07-31

fully specified name(s)

Microcephalus, complex motor and sensory axonal neuropathy syndrome (disorder)

synonyms

Microcephalus, complex motor and sensory axonal neuropathy syndrome
Microcephaly, complex motor and sensory axonal neuropathy syndrome

attributes - group1

Pathological process

Pathological developmental process 308490002

Finding site

Head structure 69536005

Occurrence

Congenital 255399007

Associated morphology

Congenital smallness 41086002

attributes - group2

Interprets

Birth head circumference 169876006

Has interpretation

Below reference range 281300000

attributes - group3

Finding site

Peripheral nervous system structure 3058005

parents

Congenital microcephaly 1148758003
Developmental hereditary disorder 363070008
Hereditary motor and sensory neuropathy 398100001
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Body measurement finding 365605003
Finding of head circumference 301338002
Microcephaly 1148757008
Congenital microcephaly 1148758003
Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008

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 peripheral neuropathy 65017003
Hereditary motor and sensory neuropathy 398100001
Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008

ancestors

sorted most to least specific

Congenital microcephaly 1148758003
Developmental hereditary disorder 363070008
Hereditary motor and sensory neuropathy 398100001
Autosomal recessive hereditary disorder 85995004
Microcephaly 1148757008
Hereditary peripheral neuropathy 65017003
Autosomal hereditary disorder 1899006
Congenital anomaly of head 87290003
Finding of head circumference 301338002
Hereditary disorder of nervous system 363235000
Disorder of head 118934005
Disorder of the peripheral nervous system 42658009
Congenital malformation 276654001
Body measurement finding 365605003
Disorder of nervous system 118940003
Head finding 406122000
Developmental disorder 5294002
Hereditary disorder by system 363137000
Congenital disease 66091009
Hereditary disease 32895009
Disorder of body system 362965005
Finding of head and neck region 118254002
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

Body measurement finding 365605003

Finding of head circumference 301338002

Microcephaly 1148757008

Congenital microcephaly 1148758003

Microcephalus, complex motor and sensory axonal neuropathy syndrome 763798008

SNOMED CT code